Organic compounds and their uses

ABSTRACT

The present application describes organic compounds that are useful for the treatment, prevention and/or amelioration of human diseases.

BACKGROUND

Chronic hepatitis C virus (HCV) infection is a major global healthburden, with an estimated 170 million people infected worldwide and anadditional 3 to 4 million infected each year (See e.g. World HealthOrganization Fact Sheet No. 164. October 2000). Although 25% of newinfections are symptomatic, 60-80% of patients will develop chronicliver disease, of whom an estimated 20% will progress to cirrhosis witha 1-4% annual risk of developing hepatocellular carcinoma (See e.g.World Health Organization Guide on Hepatitis C. 2002; Pawlotsky, J-M.(2006) Therapy of Hepatitis C: From Empiricism to Eradication.Hepatology 43:S207-S220). Overall, HCV is responsible for 50-76% of allliver cancer cases and two thirds of all liver transplants in thedeveloped world (See e.g. World Health Organization Guide on ViralCancers. 2006). And ultimately, 5-7% of infected patients will die fromthe consequences of HCV infection (See e.g. World Health OrganizationGuide on Hepatitis C. 2002).

The current standard therapy for HCV infection is pegylated interferonalpha (IFN-α) in combination with ribavirin. However, only up to 50% ofpatients with genotype 1 virus can be successfully treated with thisinterferon-based therapy. Moreover, both interferon and ribavirin caninduce significant adverse effects, ranging from flu-like symptoms(fever and fatigue), hematologic complications (leukopenia,thrombocytopenia), neuropsychiatric issues (depression, insomnia,irritability), weight loss, and autoimmune dysfunctions (hypothyroidism,diabetes) from treatment with interferon to significant hemolytic anemiafrom treatment with ribavirin. Therefore, more effective and bettertolerated drugs are still greatly needed.

NS3, an approximately 70 kDa protein, has two distinct domains: aN-terminal serine protease domain of 180 amino acids (AA) and aC-terminal helicase/NTPase domain (AA 181 to 631). The NS3 protease isconsidered a member of the chymotrypsin family because of similaritiesin protein sequence, overall three-dimensional structure and mechanismof catalysis. The HCV NS3 serine protease is responsible for proteolyticcleavage of the polyprotein at the NS3/NS4A, NS4A/NS4B, NS4B/NS5A andNS5A/NS5B junctions (See e.g. Bartenschlager, R., L. et al. (1993) J.Virol. 67:3835-3844; Grakoui, A. et al. (1993) J. Virol. 67:2832-2843;Tomei, L. et al. (1993) J. Virol. 67:4017-4026). NS4A, an approximately6 kDa protein of 54 AA, is a co-factor for the serine protease activityof NS3 (See e.g. Failla, C. et al. (1994) J. Virol. 68:3753-3760; Tanji,Y. et al. (1995) J. Virol. 69:1575-1581). Autocleavage of the NS3/NS4Ajunction by the NS3/NS4A serine protease occurs intramolecularly (i.e.,cis) while the other cleavage sites are processed intermolecularly(i.e., trans). It has been demonstrated that HCV NS3 protease isessential for viral replication and thus represents an attractive targetfor antiviral chemotherapy.

There remains a need for new treatments and therapies for HCV infection,as well as HCV-associated disorders. There is also a need for compoundsuseful in the treatment or prevention or amelioration of one or moresymptoms of HCV, as well as a need for methods of treatment orprevention or amelioration of one or more symptoms of HCV. Furthermore,there is a need for new compounds capable of modulating the activity ofHCV-serine proteases, particularly the HCV NS3/NS4a serine protease andusing said compounds to treat, prevent or ameliorate HCV infection.

SUMMARY OF THE INVENTION

In one aspect, the invention provides compounds of Formula I:

and isomers and pharmaceutically acceptable salts, hydrates, andsolvates thereof.

In one embodiment, the invention provides a method of treating anHCV-associated disorder comprising administering to a subject in needthereof a pharmaceutically acceptable amount of a compound of theinvention, such that the HCV-associated disorder is treated.

In another embodiment, the invention provides a method of treating anHIV infection comprising administering to a subject in need thereof apharmaceutically acceptable amount of a compound of the invention.

In still another embodiment, the invention provides a method oftreating, inhibiting or preventing the activity of HCV in a subject inneed thereof, comprising administering to the subject a pharmaceuticallyacceptable amount of a compound of the invention. In one embodiment, thecompounds of the invention inhibit the activity of the NS2 protease, theNS3 protease, the NS3 helicase, the NS5a protein, and/or the NS5bpolymerase. In another embodiment, the interaction between the NS3protease and NS4A cofactor is disrupted. In yet another embodiment, thecompounds of the invention prevent or alter the severing of one or moreof the NS4A-NS4B, NS4B-NS5A and NS5A-NS5B junctions of the HCV. Inanother embodiment, the invention provides a method of inhibiting theactivity of a serine protease, comprising the step of contacting saidserine protease with a compound of the invention. In another embodiment,the invention provides a method of treating, inhibiting or preventingthe activity of HCV in a subject in need thereof, comprisingadministering to the subject a pharmaceutically acceptable amount of acompound of the invention, wherein the compound interacts with anytarget in the HCV life cycle. In one embodiment, the target of the HCVlife cycle is selected from the group consisting of NS2 protease, NS3protease, NS3 helicase, NS5a protein and NS5b polymerase.

In another embodiment, the invention provides a method of decreasing theHCV RNA load in a subject in need thereof comprising administering tothe subject a pharmaceutically acceptable amount of a compound of theinvention.

In another embodiment, the compounds of the invention exhibit HCVprotease activity. In one embodiment, the compounds are an HCV NS3-4Aprotease inhibitor.

In another embodiment, the invention provides a method of treating anHCV-associated disorder in a subject, comprising administering to asubject in need thereof a pharmaceutically acceptable amount of acompound of the invention, and a pharmaceutically acceptable carrier,such that the HCV-associated disorder is treated.

In still another embodiment, the invention provides a method of treatingan HCV-associated disorder comprising administering to a subject in needthereof a pharmaceutically effective amount of a compound of theinvention, in combination with a pharmaceutically effective amount of anadditional HCV-modulating compound, such as interferon or derivatizedinterferon, or a cytochrome P450 monooxygenase inhibitor, such that theHCV-associated disorder is treated. In one embodiment, the additionalHCV-modulating compound is selected from the group consisting of NIM811,ITMN191, MK-7009, TMC 435350, Sch 503034 and VX-950.

In another embodiment, the invention provides a method of inhibitinghepatitis C virus replication in a cell, comprising contacting said cellwith a compound of the invention.

In yet another embodiment, the invention provides a packagedHCV-associated disorder treatment, comprising an HCV-modulating compoundof the invention, packaged with instructions for using an effectiveamount of the HCV-modulating compound to treat an HCV-associateddisorder.

In certain embodiments, the HCV-associated disorder is selected from thegroup consisting of HCV infection, liver cirrhosis, chronic liverdisease, hepatocellular carcinoma, cryoglobulinaemia, non-Hodgkin'slymphoma, liver fibrosis and a suppressed innate intracellular immuneresponse.

In another embodiment, the invention provides a method of treating HCVinfection, liver cirrhosis, chronic liver disease, hepatocellularcarcinoma, cryoglobulinaemia, non-Hodgkin's lymphoma, liver fibrosisand/or a suppressed innate intracellular immune response in subject inneed thereof comprising administering to the subject a pharmaceuticallyacceptable amount of a compound of the invention.

In one embodiment, the HCV to be treated is selected of any HCVgenotype. In another embodiment, the HCV is selected from HCV genotype1, 2 and/or 3.

Various embodiments of the invention are described herein. It will berecognized that features specified in each embodiment may be combinedwith other specified features to provide further embodiments.

Other aspects of the invention are discussed infra.

DETAILED DESCRIPTION OF THE INVENTION

This invention is directed to compounds, e.g., peptide compounds, andintermediates thereto, as well as pharmaceutical compositions containingthe compounds for use in treatment of HCV infection. This invention isalso directed to the compounds of the invention or compositions thereofas protease inhibitors, particularly as serine protease inhibitors, andmore particularly as HCV NS3 protease inhibitors. The compounds areparticularly useful in interfering with the life cycle of the hepatitisC virus and in treating or preventing an HCV infection or physiologicalconditions associated therewith. The present invention is also directedto methods of combination therapy for inhibiting HCV replication incells, or for treating or preventing an HCV infection in patients usingthe compounds of the invention or pharmaceutical compositions, or kitsthereof.

Certain compounds of the instant invention include those compounds ofFormula (I):

and pharmaceutically acceptable salts and stereoisomers thereof;

wherein

R is C₁-C₆alkyl, C₂-C₆alkenyl or C₃-C₇cycloalkylC₀-C₄alkyl;

R′ is hydrogen or C₁-C₆alkyl; or

R and R′, together with the carbon atom to which they are attached, forma three to seven member carbocycle which is saturated or partiallyunsaturated, which carbocycle is substituted with 0, 1, 2, or 3 residuesindependently selected from the group consisting of C₁-C₆alkyl,C₂-C₆alkenyl, C₁-C₄alkylidenyl, and C₃-C₇cycloalkylC₀-C₄alkyl;

R₁ and R₂ are independently hydrogen or are independently selected fromthe group consisting of C₁-C₆alkyl, C₁-C₆alkoxy andC₃-C₇cycloalkylC₀-C₂alkyl, each of which is substituted with 0, 1, or 2residues selected from halogen and C₁-C₄alkyl; or

R₁ and R₂, taken in combination with the N to which they are attached,form a saturated, unsaturated or aromatic heterocyclic ring having 0, 1,or 2 additional ring heteroatoms independently selected from N, O, or Sand which heterocyclic ring has from 4 to 7 total ring atoms, saidheterocycle having 0, 1, 2, or 3 substituents which are independentlyselected from C₁-C₄alkyl, halo C₁-C₄alkyl, C₂-C₄alkenyl, C₂-C₄alkynyl,hydroxyl, C₁-C₄alkoxy, haloC₁-C₄alkoxy, amino, mono- anddi-C₁₋₄alkylamino, C₁-C₄alkanoylaminoC₁-C₄alkyl;

R₄ is C₁-C₈alkyl, C₃-C₈cycloalkyl, or saturated 5 or 6 memberedheterocyclic ring having 1 or 2 ring heteroatoms independently selectedfrom N, O or S, each of which is substituted with 0-2 C₁-C₄alkyl groups;

J is a bond or a divalent residue of the formula:

R₅ is C₁-C₈alkyl, C₃-C₈cycloalkyl, or saturated 5 or 6 memberedheterocyclic ring having 1 or 2 ring heteroatoms independently selectedfrom N, O or S, each of which is substituted with 0-2 C₁-C₄alkyl groups;

R₆ is hydrogen or C₁-C₄alkyl;

G is a group of the formula -E-R₇;

E is a bond, CH₂, C(O), S(O)₂, C(R₉)₂C(O), or C(O)C(R₉)₂,

R₇ is selected from the group consisting of C₁-C₆alkyl, haloC₁-C₆alkyl,C₃-C₇cycloalkylC₀-C₂alkyl, C₁-C₆alkoxy, haloC₁-C₆alkoxy,C₃-C₇cycloalkylC₀-C₂alkoxy, mono- and di-C₁-C₆alkylamino, —S(O)₂R₁₀,—N(R₉)S(O)₂R₁₀, monocyclic or bicyclic heterocycle, and monocyclic orbicyclic aryl, wherein each residue is unsubstituted or substituted with1, 2, or 3 R₈ groups each of which R₈ residues is independently selectedfrom the group consisting of C₁-C₆alkyl, and C₁-C₆alkanoyl; or

R₆ and R₇, taken in combination with the N atom to which they areattached, forms a 4 to 7 membered heterocyclic ring having 0, 1, or 2additional ring heteroatoms selected from N, O or S and which ring issubstituted by 0, 1, 2 or 3 substituents which are independentlyselected from the group consisting of oxo, C₁-C₄alkyl, halo C₁-C₄alkyl,C₂-C₄alkenyl, C₂-C₄alkynyl, hydroxyl, C₁-C₄alkoxy, haloC₁-C₄alkoxy,amino, mono- and di-C₁₋₄alkylamino, aminoC₁-C₄alkyl,C₁-C₄alkanoylaminoC₁-C₄alkyl;

R₉ is independently selected at each occurrence from hydrogen andC₁-C₄alkyl;

R₁₀ is C₁-C₆alkyl, amino or mono- and di-C₁-C₆alkylamino; andpharmaceutically acceptable salts, hydrates, and solvates thereof.

Certain compounds of Formula I provided by the invention includecompounds of Formula (II):

wherein R₃ is C₁-C₆alkyl or C₂-C₆alkenyl.

Certain other compounds of Formula I or Formula II provided by theinvention include compounds of Formula (III):

and pharmaceutically acceptable salts and stereoisomers thereof;

wherein

X is absent or selected from NR^(11a) or oxygen;

i and k are independently selected integers selected from the groupconsisting of 0, 1, 2, 3 and 4;

j is an integer selected from the group consisting of 1, 2, 3 and 4,wherein the sum of i+j+k is less than or equal to 5 and greater than orequal to 2 when X is absent and the sum of i+j+k is less than or equalto 4 and greater than or equal to 1 when X is oxygen;

R¹¹ represents zero to three residues each independently selected ateach occurrence from the group consisting of halogen, hydroxy, amino,C₁₋₄alkyl, C₃₋₆cycloalkyl, C₁₋₄alkoxy, mono- and di-C₁₋₄alkylamino,hydroxyC₁₋₄alkyl, and C₁₋₄alkoxyC₁₋₄alkyl; and

R^(11a) is independently selected at each occurrence from the groupconsisting of hydrogen, C₁₋₄alkyl, haloC₁₋₄alkyl, C₃₋₆cycloalkyl,hydroxyC₁₋₄alkyl, and C₁₋₄alkoxyC₁₋₄alkyl.

Certain compounds of Formula I, II or III provided by the inventioninclude compounds of Formula (IV):

and pharmaceutically acceptable salts and stereoisomers thereof;

wherein

i is an integer selected from the group consisting of 0, 1, 2, 3 and 4;

j is an integer selected from the group consisting of 1, 2, 3 and 4,wherein the sum of i+j is less than or equal to 5 and greater than orequal to 2;

represents zero to three residues each independently selected at eachoccurrence from the group consisting of halogen, hydroxy, amino,C₁₋₄alkyl, C₃₋₆cycloalkyl, C₁₋₄alkoxy, mono- and di-C₁₋₄alkylamino,hydroxyC₁₋₄alkyl, and C₁₋₄alkoxyC₁₋₄alkyl; and

R^(11a) is independently selected at each occurrence from the groupconsisting of hydrogen, C₁₋₄alkyl, haloC₁₋₄alkyl, C₃₋₆cycloalkyl,hydroxyC₁₋₄alkyl, and C₁₋₄alkoxyC₁₋₄alkyl.

Certain other compounds of Formula I, II, III, or IV provided by theinvention include compounds of Formula (V):

and pharmaceutically acceptable salts and stereoisomers thereof;

wherein

i is 0 or 1; and

R^(11a) is hydrogen or C₁₋₄alkyl.

In certain compounds of Formula I, II, III, IV, or V provided by theinvention, residue J is a divalent residue of the formula:

wherein R₅ is C₁-C₆alkyl, C₄-C₇cycloalkyl, or saturated 5 or 6 memberedheterocyclic ring having 1 or 2 ring heteroatoms independently selectedfrom N, O or S, each of which is substituted with 0-2 C₁-C₄ alkylgroups.

Certain other compounds of Formula I, II, III, IV or V provided by theinvention include compounds of Formula (VI):

wherein R₁ and R₂ are independently selected from C₁C₄alkyl,C₃-C₆cycloalkyl, cyclopropylmethyl, and haloC₁-C₄alkyl, or R₁, R₂ andthe nitrogen atom to which they are attached form a pyrrolidinyl ring, apiperidinyl ring or a morpholinyl ring. In certain other compounds ofFormula VI, R₁ and R₂ are ethyl-d₅, or R₁, R₂ and the nitrogen atom towhich they are attached form pyrrolidinyl-d₈;R₃ is ethyl or vinyl;R₄ and R₅ are independently selected from the group consisting oftert-butyl, cyclohexyl, 1-methyl-cyclohexyl, tetrahydropyran-4-yl and1-methyl-tetrahydropyran-4-yl;R_(11a) is selected from C₁-C₄ alkyl, or R_(11a) is ethyl, isopropyl,ethyl-d₅, or isopropyl-d₅; and i is 0 or 1.

In certain compounds of Formula I, II, III, IV, or V provided by theinvention, residues R₄ and R₅ are independently selected from the groupconsisting of tert-butyl, cyclohexyl, 1-methyl-cyclohexyl,tetrahydropyran-4-yl and 1-methyl-tetrahydropyran-4-yl.

Certain compounds of Formula I, II, III, IV, or V provided by theinvention, include those compounds in which R₁ and R₂ are independentlyselected from the group consisting of hydrogen, C₁-C₆alkyl, andC₃-C₇cycloalkylC₀-C₂alkyl, or R₁ and R₂, taken in combination with the Nto which they are attached, form a saturated, unsaturated or aromaticheterocyclic ring having 0, 1, or 2 additional ring heteroatomsindependently selected from N, O, or S and which heterocyclic ring hasfrom 4 to 7 total ring atoms, said heterocycle having 0, 1, 2, or 3substituents which are independently selected from C₁-C₄alkyl, haloC₁-C₄alkyl, C₂-C₄alkenyl, C₂-C₄alkynyl, hydroxyl, C₁-C₄alkoxy,haloC₁-C₄alkoxy, amino, mono- and di-C₁₋₄alkylamino, aminoC₁-C₄alkyl,C₁-C₄alkanoylaminoC₁-C₄alkyl.

Certain compounds of Formula I, II, III, IV, or V provided by theinvention, include those compounds in which R₁ and R₂ are independentlyselected from the group consisting of C₁-C₄alkyl, C₁-C₃alkyl substitutedwith one or more fluorine atoms, C₃-C₆cycloalkyl and cyclopropylmethyl;or R₁, R₂ and the nitrogen atom to which they are attached form apyrrolidinyl ring, a piperidinyl ring or a morpholinyl ring. In certainother compounds of Formula I, II, III, IV or V, R₁ and R₂ areindependently selected from methyl, ethyl, ethyl-d₅, propyl, isopropyl,isopropyl-d₇, or tert-butyl; or R₁, R₂ and the nitrogen atom to whichthey are attached form a pyrrolidinyl ring or anocta-deutero-pyrrolidinyl ring,

Certain compounds of Formula I provided by the invention, include thosecompounds in which R is C₁-C₆alkyl, C₂-C₄alkenyl orC₃-C₆cycloalkylC₀-C₂alkyl;

R′ is hydrogen or C₁-C₄alkyl; or

R and R′, together with the carbon atom to which they are attached, forma cyclopropyl ring, which is substituted with 0 or 1 residues selectedfrom the group consisting of C₁-C₄alkyl, C₂-C₄alkenyl, methylidene, andC₃-C₆cycloalkylC₀-C₂alkyl.

In certain compounds of Formula III, IV, or V provided by the invention,residue R_(11a) is selected from the group consisting of C₁-C₄alkyl andperdeuteroC₁-C₄alkyl. Still other compounds of Formula III, IV or Vinclude those compounds in which R_(11a) is selected from the groupconsisting of ethyl, ethyl-d₅, isopropyl and isopropyl-d₇.

Preferred embodiments of the compounds of the invention (includingpharmaceutically acceptable salts thereof, as well as enantiomers,stereoisomers, rotamers, tautomers, diastereomers, or racemates thereof)are provided in Examples 1-19 and in Tables A and Table B, and are alsoconsidered to be “compounds of the invention.” Certain preferredcompounds of the invention include but are not limited to:

-   (5R,8S)-7-[(2S)-2-{[(2S)-2-cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2-yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1-[(pyrrolidin-1-ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8-carboxamide;-   (5R,8S)-7-[(2S)-2-{[(2S)-2-cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2-yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N-{(1R,2R)-2-ethyl-1-[(pyrrolidin-1-ylsulfonyl)carbamoyl]cyclopropyl}-10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8-carboxamide;-   (5R,8S)-7-[(2S)-2-{[(2S)-2-cyclohexyl-2-({[(2S)-1-ethylpyrrolidin-2-yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N-[(1R,2S)-1-{[(diethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]-10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8-carboxamide;-   (5R,8S)-7-[(2S)-2-{[(2S)-2-cyclohexyl-2-({[(2S)-1-ethylpyrrolidin-2-yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N-[(1R,2R)-1-{[(diethylamino)sulfonyl]carbamoyl}-2-ethylcyclopropyl]-10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8-carboxamide;-   (5R,8S)-7-[(2S)-2-{[(2S)-2-cyclohexyl-2-({[(2S)-1-ethylpyrrolidin-2-yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1-[(piperidin-1-ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8-carboxamide;-   (5R,8S)-7-[(2S)-2-{[(2S)-2-cyclohexyl-2-({[(2S)-1-ethylpyrrolidin-2-yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N-{(1R,2R)-2-ethyl-1-[(pyrrolidin-1-ylsulfonyl)carbamoyl]cyclopropyl}-10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8-carboxamide;-   (5R,8S)-7-[(2S)-2-({cyclohexyl[(pyridin-4-ylacetyl)amino]acetyl}amino)-3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1-[(pyrrolidin-1-ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8-carboxamide;-   (5R)-7-[(2S)-2-[(N-{[(2S)-1-isopropylpiperidin-2-yl]carbonyl}-3-methyl-L-valyl)amino]-2-(tetrahydro-2H-pyran-4-yl)acetyl]-10,10-dimethyl-N-{(1R,2S)-1-[(pyrrolidin-1-ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8-carboxamide;-   (5R,8S)-7-[(2S)-2-{[(2S)-2-cyclohexyl-2-({[(2S)-1-ethylpiperidin-2-yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1-[(pyrrolidin-1-ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8-carboxamide;    and-   (5R,8S)-7-[(2S)-2-{[(2S)-2-cyclohexyl-2-({[(2S)-1-isopropylpyrrolidin-2-yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1-[(pyrrolidin-1-ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8-carboxamide.

Using the HCV NS3-4A protease and Luciferase-HCV replicon assaysdescribed in the exemplification section below, the compounds of theinvention are found to show IC₅₀ values for HCV inhibition in the rangefrom 0.1 to more than 100 nM, or 0.5 to 30 nM, including, for example,the range from 0.5 to 10 nM or less.

In certain embodiments, a compound of the present invention is furthercharacterized as a modulator of HCV, including a mammalian HCV, andespecially including a human HCV. In a preferred embodiment, thecompound of the invention is an HCV inhibitor.

The terms “HCV-associated state” or “HCV-associated disorder” includedisorders and states (e.g., a disease state) that are associated withthe activity of HCV, e.g., infection of HCV in a subject. HCV-associatedstates include HCV-infection, liver cirrhosis, chronic liver disease,hepatocellular carcinoma, cryoglobulinaemia, non-Hodgkin's lymphoma,liver fibrosis and a suppressed innate intracellular immune response.

HCV-associated states are often associated with the NS3 serine proteaseof HCV, which is responsible for several steps in the processing of theHCV polyprotein into smaller functional proteins. NS3 protease forms aheterodimeric complex with the NS4A protein, an essential cofactor thatenhances enzymatic activity, and is believed to help anchor HCV to theendoplasmic reticulum. NS3 first autocatalyzes hydrolysis of theNS3-NS4A juncture, and then cleaves the HCV polyprotein intermolecularlyat the NS4A-NS4B, NS4B-NS5A and NS5A-NS5B intersections. This process isassociated with replication of HCV in a subject. Inhibiting ormodulating the activity of one or more of the NS3, NS4A, NS4B, NS5A andNS5B proteins will inhibit or modulate replication of HCV in a subject,thereby preventing or treating the HCV-associated state. In a particularembodiment, the HCV-associated state is associated with the activity ofthe NS3 protease. In another particular embodiment, the HCV-associatedstate is associated with the activity of NS3-NS4A heterodimeric complex.

In one embodiment, the compounds of the invention are NS3/NS4A proteaseinhibitors. In another embodiment, the compounds of the invention areNS2/NS3 protease inhibitors.

Without being bound by theory, it is believed that the disruption of theabove protein-protein interactions by the compounds of the inventionwill interfere with viral polyprotein processing by the NS3 protease andthus viral replication.

HCV-associated disorders also include HCV-dependent diseases.HCV-dependent diseases include, e.g., any disease or disorder thatdepend on or related to activity or misregulation of at least one strainof HCV.

The present invention includes treatment of HCV-associated disorders asdescribed above, but the invention is not intended to be limited to themanner by which the compound performs its intended function of treatmentof a disease. The present invention includes treatment of diseasesdescribed herein in any manner that allows treatment to occur, e.g., HCVinfection.

In a related embodiment, the compounds of the invention can be usefulfor treating diseases related to HIV, as well as HIV infection and AIDS(Acquired Immune Deficiency Syndrome).

In certain embodiments, the invention provides a pharmaceuticalcomposition of any of the compounds of the present invention. In arelated embodiment, the invention provides a pharmaceutical compositionof any of the compounds of the present invention and a pharmaceuticallyacceptable carrier or excipient of any of these compounds. In certainembodiments, the invention includes the compounds as novel chemicalentities.

In one embodiment, the invention includes a packaged HCV-associateddisorder treatment. The packaged treatment includes a compound of theinvention packaged with instructions for using an effective amount ofthe compound of the invention for an intended use.

The compounds of the present invention are suitable as active agents inpharmaceutical compositions that are efficacious particularly fortreating HCV-associated disorders. The pharmaceutical composition invarious embodiments has a pharmaceutically effective amount of thepresent active agent along with other pharmaceutically acceptableexcipients, carriers, fillers, diluents and the like. The phrase,“pharmaceutically effective amount” as used herein indicates an amountnecessary to administer to a host, or to a cell, issue, or organ of ahost, to achieve a therapeutic result, especially an anti-HCV effect,e.g., inhibition of proliferation of the HCV virus, or of any otherHCV-associated disease.

In one embodiment, the diseases to be treated by compounds of theinvention include, for example, HCV infection, liver cirrhosis, chronicliver disease, hepatocellular carcinoma, cryoglobulinaemia,non-Hodgkin's lymphoma, liver fibrosis and a suppressed innateintracellular immune response.

In other embodiments, the present invention provides a method forinhibiting the activity of HCV. The method includes contacting a cellwith any of the compounds of the present invention. In a relatedembodiment, the method further provides that the compound is present inan amount effective to selectively inhibit the activity of one or moreof the NS3, NS4A, NS4B, NS5A and NS5B proteins. In another relatedembodiment, the method provides that the compound is present in anamount effective to diminish the HCV RNA load in a subject.

In other embodiments, the present invention provides a use of any of thecompounds of the invention for manufacture of a medicament to treat HCVinfection in a subject.

In other embodiments, the invention provides a method of manufacture ofa medicament, including formulating any of the compounds of the presentinvention for treatment of a subject.

DEFINITIONS

The term “treat,” “treated,” “treating” or “treatment” includes thediminishment or alleviation of at least one symptom associated or causedby the state, disorder or disease being treated. In certain embodiments,the treatment comprises the induction of an HCV-inhibited state,followed by the activation of the HCV-modulating compound, which wouldin turn diminish or alleviate at least one symptom associated or causedby the HCV-associated state, disorder or disease being treated. Forexample, treatment can be diminishment of one or several symptoms of adisorder or complete eradication of a disorder.

The term “subject” is intended to include organisms, e.g., prokaryotesand eukaryotes, which are capable of suffering from or afflicted with anHCV-associated disorder. Examples of subjects include mammals, e.g.,humans, dogs, cows, horses, pigs, sheep, goats, cats, mice, rabbits,rats, and transgenic non-human animals. In certain embodiments, thesubject is a human, e.g., a human suffering from, at risk of sufferingfrom, or potentially capable of suffering from an HCV-associateddisorder, and for diseases or conditions described herein, e.g., HCVinfection. In another embodiment, the subject is a cell.

The language “HCV-modulating compound,” “modulator of HCV” or “HCVinhibitor” refers to compounds that modulate, e.g., inhibit, orotherwise alter, the activity of HCV. Similarly, an “NS3/NS4A proteaseinhibitor,” or an “NS2/NS3 protease inhibitor” refers to a compound thatmodulates, e.g., inhibits, or otherwise alters, the interaction of theseproteases with one another. Examples of HCV-modulating compounds includecompounds of Formula I, subformulae thereof, as well as compounds ofExamples 1-19 and Tables A and B (including pharmaceutically acceptablesalts thereof, as well as enantiomers, stereoisomers, rotamers,tautomers, diastereomers, or racemates thereof).

Additionally, the method includes administering to a subject aneffective amount of an HCV-modulating compound of the invention, e.g.,HCV-modulating compounds of Formula I or Formula III, as well as Table A(including salts thereof, e.g., pharmaceutically acceptable saltsthereof, as well as enantiomers, stereoisomers, rotamers, tautomers,diastereomers, or racemates thereof).

Unless indicated otherwise, the nomenclature of substituents that arenot explicitly defined herein are arrived at by naming the terminalportion of the functionality followed by the adjacent functionalitytoward the point of attachment. For example, the substituent“arylalkyloxycarbonyl” refers to the group (aryl)-(alkyl)-O—C(O)—.

It is understood that in all substituted groups defined above, polymersarrived at by defining substituents with further substituents tothemselves are not intended for inclusion herein. In such cases, themaximum number of such substitutions is three. For example, serialsubstitutions of substituted aryl groups with two other substituted arylgroups are limited to—substituted aryl-(substituted aryl)-substitutedaryl.

Similarly, it is understood that the above definitions are not intendedto include impermissible substitution patterns (e.g., methyl substitutedwith 5 fluoro groups). Such impermissible substitution patterns are wellknown to the skilled artisan.

The term “alkyl” includes saturated aliphatic groups, includingstraight-chain alkyl groups (e.g., methyl, ethyl, propyl, butyl, pentyl,hexyl, heptyl, octyl, nonyl, decyl, etc.), branched-chain alkyl groups(isopropyl, tert-butyl, isobutyl, etc.), cycloalkyl (alicyclic) groups(cyclopropyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl), alkylsubstituted cycloalkyl groups, and cycloalkyl substituted alkyl groups.Furthermore, the expression “C_(x)-C_(y)-alkyl”, wherein x is 1-5 and yis 2-10 indicates a particular alkyl group (straight- or branched-chain)of a particular range of carbons. For example, the expressionC₁-C₄-alkyl includes, but is not limited to, methyl, ethyl, propyl,butyl, isopropyl, tert-butyl, isobutyl and sec-butyl. Moreover, the termC₃₋₆-cycloalkyl includes, but is not limited to, cyclopropyl,cyclopentyl, and cyclohexyl. As discussed below, these alkyl groups, aswell as cycloalkyl groups, may be further substituted. “C₀-C_(n)alkyl”refers to a single covalent bond (Co) or an alkyl group having from 1 ton carbon atoms; for example “C₀-C₄alkyl” refers to a single covalentbond or a C₁-C₄alkyl group; “C₀-C₈alkyl” refers to a single covalentbond or a C₁-C₈alkyl group. In some instances, a substituent of an alkylgroup is specifically indicated. For example, “C₁-C₄ hydroxyalkyl”refers to a C₁-C₄alkyl group that has at least one hydroxy substituent.

“Alkylene” refers to a divalent alkyl group, as defined above.C₀-C₄alkylene is a single covalent bond or an alkylene group having from1 to 4 carbon atoms; and C₀-C₆alkylene is a single covalent bond or analkylene group having from 1 to 6 carbon atoms.

A “cycloalkyl” is a group that comprises one or more saturated and/orpartially saturated rings in which all ring members are carbon, such ascyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl,cyclooctyl, adamantyl, decahydro-naphthalenyl, octahydro-indenyl, andpartially saturated variants of the foregoing, such as cyclohexenyl.Cycloalkyl groups do not comprise an aromatic ring or a heterocyclicring. Certain cycloalkyl groups are C₃-C₈cycloalkyl, in which the groupcontains a single ring with from 3 to 8 ring members. A“(C₃-C₈cycloalkyl)C₀-C₄alkyl” is a C₃-C₈cycloalkyl group linked via asingle covalent bond or a C₁-C₄alkylene group.

Moreover, alkyl (e.g., methyl, ethyl, propyl, butyl, pentyl, hexyl,etc.) include both “unsubstituted alkyl” and “substituted alkyl”, thelatter of which refers to alkyl moieties having substituents replacing ahydrogen on one or more carbons of the hydrocarbon backbone, which allowthe molecule to perform its intended function.

The term “substituted” is intended to describe moieties havingsubstituents replacing a hydrogen on one or more atoms, e.g. C, O or N,of a molecule. Such substituents can include, for example, alkenyl,alkynyl, halogen, hydroxyl, alkylcarbonyloxy, arylcarbonyloxy,alkoxycarbonyloxy, aryloxycarbonyloxy, carboxylate, alkylcarbonyl,arylcarbonyl, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl,dialkylaminocarbonyl, alkylthiocarbonyl, alkoxyl, phosphate,phosphonato, phosphinato, amino (including alkyl amino, dialkylamino,arylamino, diarylamino, and alkylarylamino), acylamino (includingalkylcarbonylamino, arylcarbonylamino, carbamoyl and ureido), amidino,imino, sulfhydryl, alkylthio, arylthio, thiocarboxylate, sulfates,alkylsulfinyl, sulfonato, sulfamoyl, sulfonamido, nitro,trifluoromethyl, cyano, azido, heterocyclyl, alkylaryl, morpholino,phenol, benzyl, phenyl, piperazine, cyclopentane, cyclohexane, pyridine,5H-tetrazole, triazole, piperidine, or an aromatic or heteroaromaticmoiety.

Further examples of substituents of the invention, which are notintended to be limiting, include moieties selected from straight orbranched alkyl (preferably C₁-C₅), cycloalkyl (preferably C₃-C₈), alkoxy(preferably C₁-C₆), thioalkyl (preferably C₁-C₆), alkenyl (preferablyC₂-C₆), alkynyl (preferably C₂-C₆), heterocyclic, carbocyclic, aryl(e.g., phenyl), aryloxy (e.g., phenoxy), aralkyl (e.g., benzyl),aryloxyalkyl (e.g., phenyloxyalkyl), arylacetamidoyl, alkylaryl,heteroaralkyl, alkylcarbonyl and arylcarbonyl or other such acyl group,heteroarylcarbonyl, or heteroaryl group, (CR′R″)₀₋₃NR′R″ (e.g., —NH₂),(CR′R″)₀₋₃CN (e.g., —CN), —NO₂, halogen (e.g., —F, —Cl, —Br, or —I),(CR′R″)₀₋₃C(halogen)₃ (e.g., —CF₃), (CR′R″)₀₋₃CH(halogen)₂,(CR′R″)₀₋₃CH₂(halogen), (CR′R″)₀₋₃CONR′R″, (CR′R″)₀₋₃(CNH)NR′R″,(CR′R″)₀₋₃S(O)₁₋₂NR′R″, (CR′R″)₀₋₃CHO, (CR′R″)₀₋₃₀(CR′R″)₀₋₃H,(CR′R″)₀₋₃S(O)₀₋₃R′ (e.g., —SO₃H, —OSO₃H), (CR′R″)₀₋₃O(CR′R″)₀₋₃H (e.g.,—CH₂OCH₃ and —OCH₃), (CR′R″)₀₋₃S(CR′R″)₀₋₃H (e.g., —SH and —SCH₃),(CR′R″)₀₋₃OH (e.g., —OH), (CR′R″)₀₋₃COR′, (CR′R″)₀₋₃ (substituted orunsubstituted phenyl), (CR′R″)₀₋₃(C₃-C₈cycloalkyl), (CR′R″)₀₋₃CO₂R′(e.g., —CO₂H), or (CR′R″)₀₋₃OR′ group, or the side chain of anynaturally occurring amino acid; wherein R′ and R″ are each independentlyhydrogen, a C₁-C₅ alkyl, C₂-C₅ alkenyl, C₂-C₅ alkynyl, or aryl group.Such substituents can include, for example, halogen, hydroxyl,alkylcarbonyloxy, arylcarbonyloxy, alkoxycarbonyloxy,aryloxycarbonyloxy, carboxylate, alkylcarbonyl, alkoxycarbonyl,aminocarbonyl, alkylthiocarbonyl, alkoxyl, phosphate, phosphonato,phosphinato, cyano, amino (including alkyl amino, dialkylamino,arylamino, diarylamino, and alkylarylamino), acylamino (includingalkylcarbonylamino, arylcarbonylamino, carbamoyl and ureido), amidino,imino, oxime, sulfhydryl, alkylthio, arylthio, thiocarboxylate,sulfates, sulfonato, sulfamoyl, sulfonamido, nitro, trifluoromethyl,cyano, azido, heterocyclyl, or an aromatic or heteroaromatic moiety. Incertain embodiments, a carbonyl moiety (C═O) may be further derivatizedwith an oxime moiety, e.g., an aldehyde moiety may be derivatized as itsoxime (—C═N—OH) analog. It will be understood by those skilled in theart that the moieties substituted on the hydrocarbon chain canthemselves be substituted, if appropriate. Cycloalkyls can be furthersubstituted, e.g., with the substituents described above. An “aralkyl”moiety is an alkyl substituted with an aryl (e.g., phenylmethyl (i.e.,benzyl)).

The term “alkenyl” includes unsaturated aliphatic groups analogous inlength and possible substitution to the alkyls described above, butwhich contain at least one double bond.

For example, the term “alkenyl” includes straight-chain alkenyl groups(e.g., ethenyl, propenyl, butenyl, pentenyl, hexenyl, heptenyl, octenyl,nonenyl, decenyl, etc.), branched-chain alkenyl groups, cycloalkenyl(alicyclic) groups (cyclopropenyl, cyclopentenyl, cyclohexenyl,cycloheptenyl, cyclooctenyl), alkyl or alkenyl substituted cycloalkenylgroups, and cycloalkyl or cycloalkenyl substituted alkenyl groups. Theterm alkenyl further includes alkenyl groups that include oxygen,nitrogen, sulfur or phosphorous atoms replacing one or more carbons ofthe hydrocarbon backbone. In certain embodiments, a straight chain orbranched chain alkenyl group has 6 or fewer carbon atoms in its backbone(e.g., C₂-C₆ for straight chain, C₃-C₆ for branched chain). Likewise,cycloalkenyl groups may have from 3-8 carbon atoms in their ringstructure, and more preferably have 5 or 6 carbons in the ringstructure. The term C₂-C₆ includes alkenyl groups containing 2 to 6carbon atoms.

Moreover, the term alkenyl includes both “unsubstituted alkenyls” and“substituted alkenyls”, the latter of which refers to alkenyl moietieshaving substituents replacing a hydrogen on one or more carbons of thehydrocarbon backbone. Such substituents can include, for example, alkylgroups, alkynyl groups, halogens, hydroxyl, alkylcarbonyloxy,arylcarbonyloxy, alkoxycarbonyloxy, aryloxycarbonyloxy, carboxylate,alkylcarbonyl, arylcarbonyl, alkoxycarbonyl, aminocarbonyl,alkylaminocarbonyl, dialkylaminocarbonyl, alkylthiocarbonyl, alkoxyl,phosphate, phosphonato, phosphinato, cyano, amino (including alkylamino, dialkylamino, arylamino, diarylamino, and alkylarylamino),acylamino (including alkylcarbonylamino, arylcarbonylamino, carbamoyland ureido), amidino, imino, sulfhydryl, alkylthio, arylthio,thiocarboxylate, sulfates, alkylsulfinyl, sulfonato, sulfamoyl,sulfonamido, nitro, trifluoromethyl, cyano, azido, heterocyclyl,alkylaryl, or an aromatic or heteroaromatic moiety.

The term “alkynyl” includes unsaturated aliphatic groups analogous inlength and possible substitution to the alkyls described above, butwhich contain at least one triple bond.

For example, the term “alkynyl” includes straight-chain alkynyl groups(e.g., ethynyl, propynyl, butynyl, pentynyl, hexynyl, heptynyl, octynyl,nonynyl, decynyl, etc.), branched-chain alkynyl groups, and cycloalkylor cycloalkenyl substituted alkynyl groups. The term alkynyl furtherincludes alkynyl groups that include oxygen, nitrogen, sulfur orphosphorous atoms replacing one or more carbons of the hydrocarbonbackbone. In certain embodiments, a straight chain or branched chainalkynyl group has 6 or fewer carbon atoms in its backbone (e.g., C₂-C₆for straight chain, C₃-C₆ for branched chain). The term C₂-C₆ includesalkynyl groups containing 2 to 6 carbon atoms.

Moreover, the term alkynyl includes both “unsubstituted alkynyls” and“substituted alkynyls”, the latter of which refers to alkynyl moietieshaving substituents replacing a hydrogen on one or more carbons of thehydrocarbon backbone. Such substituents can include, for example, alkylgroups, alkynyl groups, halogens, hydroxyl, alkylcarbonyloxy,arylcarbonyloxy, alkoxycarbonyloxy, aryloxycarbonyloxy, carboxylate,alkylcarbonyl, arylcarbonyl, alkoxycarbonyl, aminocarbonyl,alkylaminocarbonyl, dialkylaminocarbonyl, alkylthiocarbonyl, alkoxyl,phosphate, phosphonato, phosphinato, cyano, amino (including alkylamino, dialkylamino, arylamino, diarylamino, and alkylarylamino),acylamino (including alkylcarbonylamino, arylcarbonylamino, carbamoyland ureido), amidino, imino, sulfhydryl, alkylthio, arylthio,thiocarboxylate, sulfates, alkylsulfinyl, sulfonato, sulfamoyl,sulfonamido, nitro, trifluoromethyl, cyano, azido, heterocyclyl,alkylaryl, or an aromatic or heteroaromatic moiety.

The term “amine” or “amino” should be understood as being broadlyapplied to both a molecule, or a moiety or functional group, asgenerally understood in the art, and may be primary, secondary, ortertiary. The term “amine” or “amino” includes compounds where anitrogen atom is covalently bonded to at least one carbon, hydrogen orheteroatom. The terms include, for example, but are not limited to,“alkylamino,” “arylamino,” “diarylamino,” “alkylarylamino,”“alkylaminoaryl,” “arylaminoalkyl,” “alkaminoalkyl,” “amide,” “amido,”and “aminocarbonyl.” The term “alkyl amino” comprises groups andcompounds wherein the nitrogen is bound to at least one additional alkylgroup. The term “dialkyl amino” includes groups wherein the nitrogenatom is bound to at least two additional alkyl groups. The term“arylamino” and “diarylamino” include groups wherein the nitrogen isbound to at least one or two aryl groups, respectively. The term“alkylarylamino,” “alkylaminoaryl” or “arylaminoalkyl” refers to anamino group which is bound to at least one alkyl group and at least onearyl group. The term “alkaminoalkyl” refers to an alkyl, alkenyl, oralkynyl group bound to a nitrogen atom which is also bound to an alkylgroup.

The term “amide,” “amido” or “aminocarbonyl” includes compounds ormoieties which contain a nitrogen atom which is bound to the carbon of acarbonyl or a thiocarbonyl group. The term includes “alkaminocarbonyl”or “alkylaminocarbonyl” groups which include alkyl, alkenyl, aryl oralkynyl groups bound to an amino group bound to a carbonyl group. Itincludes arylaminocarbonyl and arylcarbonylamino groups which includearyl or heteroaryl moieties bound to an amino group which is bound tothe carbon of a carbonyl or thiocarbonyl group. The terms“alkylaminocarbonyl,” “alkenylaminocarbonyl,” “alkynylaminocarbonyl,”“arylaminocarbonyl,” “alkylcarbonylamino,” “alkenylcarbonylamino,”“alkynylcarbonylamino,” and “arylcarbonylamino” are included in term“amide.” Amides also include urea groups (aminocarbonylamino) andcarbamates (oxycarbonylamino).

The term “aryl” includes aromatic groups, including 5- and 6-memberedsingle-ring aromatic groups that may include from zero to fourheteroatoms, for example, phenyl, pyrrole, furan, thiophene, thiazole,isothiaozole, imidazole, triazole, tetrazole, pyrazole, oxazole,isoxazole, pyridine, pyrazine, pyridazine, and pyrimidine, and the like.Furthermore, the term “aryl” includes multicyclic aryl groups, e.g.,tricyclic, bicyclic, e.g., naphthalene, benzoxazole, benzodioxazole,benzothiazole, benzoimidazole, benzothiophene, methylenedioxyphenyl,quinoline, isoquinoline, anthryl, phenanthryl, napthridine, indole,benzofuran, purine, benzofuran, deazapurine, or indolizine. Those arylgroups having heteroatoms in the ring structure may also be referred toas “aryl heterocycles”, “heterocycles,” “heteroaryls” or“heteroaromatics.” The aromatic ring can be substituted at one or morering positions with such substituents as described above, as forexample, alkyl, halogen, hydroxyl, alkoxy, alkylcarbonyloxy,arylcarbonyloxy, alkoxycarbonyloxy, aryloxycarbonyloxy, carboxylate,alkylcarbonyl, alkylaminoacarbonyl, aralkylaminocarbonyl,alkenylaminocarbonyl, alkylcarbonyl, arylcarbonyl, aralkylcarbonyl,alkenylcarbonyl, alkoxycarbonyl, aminocarbonyl, alkylthiocarbonyl,phosphate, phosphonato, phosphinato, cyano, amino (including alkylamino, dialkylamino, arylamino, diarylamino, and alkylarylamino),acylamino (including alkylcarbonylamino, arylcarbonylamino, carbamoyland ureido), amidino, imino, sulfhydryl, alkylthio, arylthio,thiocarboxylate, sulfates, alkylsulfinyl, sulfonato, sulfamoyl,sulfonamido, nitro, trifluoromethyl, cyano, azido, heterocyclyl,alkylaryl, or an aromatic or heteroaromatic moiety. Aryl groups can alsobe fused or bridged with alicyclic or heterocyclic rings which are notaromatic so as to form a polycycle (e.g., tetralin).

Certain aryl groups recited herein are C₆-C₁₀arylC₀-C₈alkyl groups(i.e., groups in which a 6- to 10-membered carbocyclic group comprisingat least one aromatic ring is linked via a single covalent bond or aC₁-C₈alkylene group). Such groups include, for example, phenyl andindanyl, as well as groups in which either of the foregoing is linkedvia C₁-C₈alkylene, preferably via C₁-C₄alkylene. Phenyl groups linkedvia a single covalent bond or C₁-C₆alkylene group are designatedphenylC₀-C₆alkyl (e.g., benzyl, 1-phenyl-ethyl, 1-phenyl-propyl and2-phenyl-ethyl).

The term heteroaryl, as used herein, represents a stable monocyclic orbicyclic ring of up to 7 atoms in each ring, wherein at least one ringis aromatic and contains from 1 to 4 heteroatoms selected from the groupconsisting of O, N and S. Heteroaryl groups within the scope of thisdefinition include but are not limited to: acridinyl, carbazolyl,cinnolinyl, quinoxalinyl, pyrrazolyl, indolyl, benzotriazolyl, furanyl,thienyl, benzothienyl, benzofuranyl, quinolinyl, isoquinolinyl,oxazolyl, isoxazolyl, indolyl, pyrazinyl, pyridazinyl, pyridinyl,pyrimidinyl, pyrrolyl, tetrahydroquinoline. As with the definition ofheterocycle below, “heteroaryl” is also understood to include theN-oxide derivative of any nitrogen-containing heteroaryl. In cases wherethe heteroaryl substituent is bicyclic and one ring is non-aromatic orcontains no heteroatoms, it is understood that attachment is via thearomatic ring or via the heteroatom containing ring, respectively.

The term “heterocycle” or “heterocyclyl” as used herein is intended tomean a 5- to 10-membered aromatic or nonaromatic heterocycle containingfrom 1 to 4 heteroatoms selected from the group consisting of O, N andS, and includes bicyclic groups. “Heterocyclyl” therefore includes theabove mentioned heteroaryls, as well as dihydro and tetrathydro analogsthereof. Further examples of “heterocyclyl” include, but are not limitedto the following: benzoimidazolyl, benzofuranyl, benzofurazanyl,benzopyrazolyl, benzotriazolyl, benzothiophenyl, benzoxazolyl,carbazolyl, carbolinyl, cinnolinyl, furanyl, imidazolyl, indolinyl,indolyl, indolazinyl, indazolyl, isobenzofuranyl, isoindolyl,isoquinolyl, isothiazolyl, isoxazolyl, naphthpyridinyl, oxadiazolyl,oxazolyl, oxazoline, isoxazoline, oxetanyl, pyranyl, pyrazinyl,pyrazolyl, pyridazinyl, pyridopyridinyl, pyridazinyl, pyridyl,pyrimidyl, pyrrolyl, quinazolinyl, quinolyl, quinoxalinyl,tetrahydropyranyl, tetrazolyl, tetrazolopyridyl, thiadiazolyl,thiazolyl, thienyl, triazolyl, azetidinyl, 1,4-dioxanyl,hexahydroazepinyl, piperazinyl, piperidinyl, pyridin-2-onyl,pyrrolidinyl, morpholinyl, thiomorpholinyl, dihydrobenzoimidazolyl,dihydrobenzofuranyl, dihydrobenzothiophenyl, dihydrobenzoxazolyl,dihydrofuranyl, dihydroimidazolyl, dihydroindolyl, dihydroisooxazolyl,dihydroisothiazolyl, dihydrooxadiazolyl, dihydrooxazolyl,dihydropyrazinyl, dihydropyrazolyl, dihydropyridinyl,dihydropyrimidinyl, dihydropyrrolyl, dihydroquinolinyl,dihydrotetrazolyl, dihydrothiadiazolyl, dihydrothiazolyl,dihydrothienyl, dihydrotriazolyl, dihydroazetidinyl,methylenedioxybenzoyl, tetrahydrofuranyl, and tetrahydrothienyl, andN-oxides thereof. Attachment of a heterocyclyl substituent can occur viaa carbon atom or via a heteroatom.

A “heterocycleC₀-C₈alkyl” is a heterocyclic group linked via a singlecovalent bond or C₁-C₈alkylene group. A (4- to 7-memberedheterocycle)C₀-C₈alkyl is a heterocyclic group (e.g., monocyclic orbicyclic) having from 4 to 7 ring members linked via a single covalentbond or an alkylene group having from 1 to 8 carbon atoms. A“(6-membered heteroaryl)C₀-C₈alkyl” refers to a heteroaryl group linkedvia a direct bond or C₁-C₆alkyl group.

The term “acyl” includes compounds and moieties which contain the acylradical (CH₃ CO—) or a carbonyl group. The term “substituted acyl”includes acyl groups where one or more of the hydrogen atoms arereplaced by for example, alkyl groups, alkynyl groups, halogens,hydroxyl, alkylcarbonyloxy, arylcarbonyloxy, alkoxycarbonyloxy,aryloxycarbonyloxy, carboxylate, alkylcarbonyl, arylcarbonyl,alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl,alkylthiocarbonyl, alkoxyl, phosphate, phosphonato, phosphinato, cyano,amino (including alkyl amino, dialkylamino, arylamino, diarylamino, andalkylarylamino), acylamino (including alkylcarbonylamino,arylcarbonylamino, carbamoyl and ureido), amidino, imino, sulfhydryl,alkylthio, arylthio, thiocarboxylate, sulfates, alkylsulfinyl,sulfonato, sulfamoyl, sulfonamido, nitro, trifluoromethyl, cyano, azido,heterocyclyl, alkylaryl, or an aromatic or heteroaromatic moiety.

The term “acylamino” includes moieties wherein an acyl moiety is bondedto an amino group. For example, the term includes alkylcarbonylamino,arylcarbonylamino, carbamoyl and ureido groups.

The term “alkoxy” includes substituted and unsubstituted alkyl, alkenyl,and alkynyl groups covalently linked to an oxygen atom. Examples ofalkoxy groups include methoxy, ethoxy, isopropyloxy, propoxy, butoxy,and pentoxy groups and may include cyclic groups such as cyclopentoxy.Examples of substituted alkoxy groups include halogenated alkoxy groups.The alkoxy groups can be substituted with groups such as alkenyl,alkynyl, halogen, hydroxyl, alkylcarbonyloxy, arylcarbonyloxy,alkoxycarbonyloxy, aryloxycarbonyloxy, carboxylate, alkylcarbonyl,arylcarbonyl, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl,dialkylaminocarbonyl, alkylthiocarbonyl, alkoxyl, phosphate,phosphonato, phosphinato, cyano, amino (including alkyl amino,dialkylamino, arylamino, diarylamino, and alkylarylamino), acylamino(including alkylcarbonylamino, arylcarbonylamino, carbamoyl and ureido),amidino, imino, sulfhydryl, alkylthio, arylthio, thiocarboxylate,sulfates, alkylsulfinyl, sulfonato, sulfamoyl, sulfonamido, nitro,trifluoromethyl, cyano, azido, heterocyclyl, alkylaryl, or an aromaticor heteroaromatic moieties. Examples of halogen substituted alkoxygroups include, but are not limited to, fluoromethoxy, difluoromethoxy,trifluoromethoxy, chloromethoxy, dichloromethoxy, trichloromethoxy, etc.

The term “carbonyl” or “carboxy” includes compounds and moieties whichcontain a carbon connected with a double bond to an oxygen atom, andtautomeric forms thereof. Examples of moieties that contain a carbonylinclude aldehydes, ketones, carboxylic acids, amides, esters,anhydrides, etc. The term “carboxy moiety” or “carbonyl moiety” refersto groups such as “alkylcarbonyl” groups wherein an alkyl group iscovalently bound to a carbonyl group, “alkenylcarbonyl” groups whereinan alkenyl group is covalently bound to a carbonyl group,“alkynylcarbonyl” groups wherein an alkynyl group is covalently bound toa carbonyl group, “arylcarbonyl” groups wherein an aryl group iscovalently attached to the carbonyl group. Furthermore, the term alsorefers to groups wherein one or more heteroatoms are covalently bondedto the carbonyl moiety. For example, the term includes moieties such as,for example, aminocarbonyl moieties, (wherein a nitrogen atom is boundto the carbon of the carbonyl group, e.g., an amide), aminocarbonyloxymoieties, wherein an oxygen and a nitrogen atom are both bond to thecarbon of the carbonyl group (e.g., also referred to as a “carbamate”).Furthermore, aminocarbonylamino groups (e.g., ureas) are also include aswell as other combinations of carbonyl groups bound to heteroatoms(e.g., nitrogen, oxygen, sulfur, etc. as well as carbon atoms).Furthermore, the heteroatom can be further substituted with one or morealkyl, alkenyl, alkynyl, aryl, aralkyl, acyl, etc. moieties.

The term “thiocarbonyl” or “thiocarboxy” includes compounds and moietieswhich contain a carbon connected with a double bond to a sulfur atom.The term “thiocarbonyl moiety” includes moieties that are analogous tocarbonyl moieties. For example, “thiocarbonyl” moieties includeaminothiocarbonyl, wherein an amino group is bound to the carbon atom ofthe thiocarbonyl group, furthermore other thiocarbonyl moieties include,oxythiocarbonyls (oxygen bound to the carbon atom),aminothiocarbonylamino groups, etc.

The term “ether” includes compounds or moieties that contain an oxygenbonded to two different carbon atoms or heteroatoms. For example, theterm includes “alkoxyalkyl” which refers to an alkyl, alkenyl, oralkynyl group covalently bonded to an oxygen atom that is covalentlybonded to another alkyl group.

The term “ester” includes compounds and moieties that contain a carbonor a heteroatom bound to an oxygen atom that is bonded to the carbon ofa carbonyl group. The term “ester” includes alkoxycarboxy groups such asmethoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, butoxycarbonyl,pentoxycarbonyl, etc. The alkyl, alkenyl, or alkynyl groups are asdefined above.

The term “thioether” includes compounds and moieties which contain asulfur atom bonded to two different carbon or hetero atoms. Examples ofthioethers include, but are not limited to alkthioalkyls,alkthioalkenyls, and alkthioalkynyls. The term “alkthioalkyls” includecompounds with an alkyl, alkenyl, or alkynyl group bonded to a sulfuratom that is bonded to an alkyl group. Similarly, the term“alkthioalkenyls” and alkthioalkynyls” refer to compounds or moietieswherein an alkyl, alkenyl, or alkynyl group is bonded to a sulfur atomwhich is covalently bonded to an alkynyl group.

The term “hydroxy” or “hydroxyl” includes groups with an —OH or —O⁻.

The term “halogen” includes fluorine, bromine, chlorine, iodine, etc.The term “perhalogenated” generally refers to a moiety wherein allhydrogens are replaced by halogen atoms.

The term “heteroatom” includes atoms of any element other than carbon orhydrogen. Preferred heteroatoms are nitrogen, oxygen, sulfur andphosphorus.

It is to be understood that all of the compounds of the inventiondescribed above will further include bonds between adjacent atoms and/orhydrogens as required to satisfy the valence of each atom. That is,bonds and/or hydrogen atoms are added to provide the following number oftotal bonds to each of the following types of atoms: carbon: four bonds;nitrogen: three bonds; oxygen: two bonds; and sulfur: two bonds.

Groups that are “optionally substituted” are unsubstituted or aresubstituted by other than hydrogen at one or more available positions,typically 1, 2, 3, 4 or 5 positions, by one or more suitable groups(which may be the same or different). Optional substitution is alsoindicated by the phrase “substituted with from 0 to X substituents,”where X is the maximum number of possible substituents. Certainoptionally substituted groups are substituted with from 0 to 2, 3 or 4independently selected substituents (i.e., are unsubstituted orsubstituted with up to the recited maximum number of substitutents).

It will also be noted that the substituents of some of the compounds ofthis invention include isomeric cyclic structures. It is to beunderstood accordingly that constitutional isomers of particularsubstituents are included within the scope of this invention, unlessindicated otherwise. For example, the term “tetrazole” includestetrazole, 2H-tetrazole, 3H-tetrazole, 4H-tetrazole and 5H-tetrazole.

As used herein, the term “isomers” refers to different compounds thathave the same molecular formula but differ in arrangement andconfiguration of the atoms. Also as used herein, the term “an opticalisomer” or “a stereoisomer” refers to any of the various stereo isomericconfigurations which may exist for a given compound of the presentinvention and includes geometric isomers. It is understood that asubstituent may be attached at a chiral center of a carbon atom.Therefore, the invention includes enantiomers, diastereomers orracemates of the compound. “Enantiomers” are a pair of stereoisomersthat are non-superimposable mirror images of each other. A 1:1 mixtureof a pair of enantiomers is a “racemic” mixture. The term is used todesignate a racemic mixture where appropriate. “Diastereoisomers” arestereoisomers that have at least two asymmetric atoms, but which are notmirror-images of each other. The absolute stereochemistry is specifiedaccording to the Cahn-Ingold-Prelog R-S system. When a compound is apure enantiomer the stereochemistry at each chiral carbon may bespecified by either R or S. Resolved compounds whose absoluteconfiguration is unknown can be designated (+) or (−) depending on thedirection (dextro- or levorotatory) which they rotate plane polarizedlight at the wavelength of the sodium D line. Certain of the compoundsdescribed herein contain one or more asymmetric centers and may thusgive rise to enantiomers, diastereomers, and other stereoisomeric formsthat may be defined, in terms of absolute stereochemistry, as (R)- or(S)-. The present invention is meant to include all such possibleisomers, including racemic mixtures, optically pure forms andintermediate mixtures. Optically active (R)- and (S)-isomers may beprepared using chiral synthons or chiral reagents, or resolved usingconventional techniques. If the compound contains a double bond, thesubstituent may be E or Z configuration. If the compound contains adisubstituted cycloalkyl, the cycloalkyl substituent may have a cis- ortrans-configuration. All tautomeric forms are also intended to beincluded.

As used herein, the term “pharmaceutically acceptable salts” refers tosalts that retain the biological effectiveness and properties of thecompounds of this invention and, which typically are not biologically orotherwise undesirable. In many cases, the compounds of the presentinvention are capable of forming acid and/or base salts by virtue of thepresence of amino and/or carboxyl groups or groups similar thereto.

Pharmaceutically acceptable acid addition salts can be formed withinorganic acids and organic acids, e.g., acetate, aspartate, benzoate,besylate, bromide/hydrobromide, bicarbonate/carbonate, bisufate/sulfate,camphorsulformate, chloride/hydrochloride, chlortheophyllonate, citrate,ethandisulfonate, fumarate, gluceptate, gluconate, glucuronate,hippurate, hydroiodide/iodide, isethionate, lactate, lactobionate,laurylsulfate, malate, maleate, malonate, mandelate, mesylate,methylsulphate, naphthoate, napsylate, nicotinate, nitrate,octadecanoate, oleate, oxalate, palmitate, pamoate, phosphate/hydrogenphosphate/dihydrogen phosphate, polygalacturonate, propionate, stearate,succinate, sulfosalicylate, tartrate, tosylate and trifluoroacetatesalts.

Inorganic acids from which salts can be derived include, for example,hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid,phosphoric acid, and the like.

Organic acids from which salts can be derived include, for example,acetic acid, propionic acid, glycolic acid, oxalic acid, maleic acid,malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid,benzoic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid,toluenesulfonic acid, sulfosalicylic acid, and the like.Pharmaceutically acceptable base addition salts can be formed withinorganic and organic bases.

Inorganic bases from which salts can be derived include, for example,sodium, potassium, ammonium, calcium, magnesium, iron, silver, zinc,copper and the like; particularly preferred are the ammonium, potassium,sodium, calcium and magnesium salts.

Organic bases from which salts can be derived include, for example,primary, secondary, and tertiary amines, substituted amines includingnaturally occurring substituted amines, cyclic amines, basic ionexchange resins, and the like, specifically such as, isopropylamine,benzathine, cholinate, diethanolamine, diethylamine, lysine, meglumine,piperazine and tromethamine.

The pharmaceutically acceptable salts of the present invention can besynthesized from a parent compound, a basic or acidic moiety, byconventional chemical methods. Generally, such salts can be prepared byreacting free acid forms of these compounds with a stoichiometric amountof the appropriate base (such as Na, Ca, Mg, or K hydroxide, carbonate,bicarbonate or the like), or by reacting free base forms of thesecompounds with a stoichiometric amount of the appropriate acid. Suchreactions are typically carried out in water or in an organic solvent,or in a mixture of the two. Generally, non-aqueous media like ether,ethyl acetate, ethanol, isopropanol, or acetonitrile are preferred,where practicable. Lists of additional suitable salts can be found,e.g., in “Remington's Pharmaceutical Sciences”, 20th ed., MackPublishing Company, Easton, Pa., (1985); and in “Handbook ofPharmaceutical Salts: Properties, Selection, and Use” by Stahl andWermuth (Wiley-VCH, Weinheim, Germany, 2002).

The present invention includes all pharmaceutically acceptableisotopically-labeled compounds of the invention, i.e. compounds offormula (I), wherein (1) one or more atoms are replaced by atoms havingthe same atomic number, but an atomic mass or mass number different fromthe atomic mass or mass number usually found in nature, and/or (2) theisotopic ratio of one or more atoms is different from the naturallyoccurring ratio.

Examples of isotopes suitable for inclusion in the compounds of theinvention comprises isotopes of hydrogen, such as ²H and ³H, carbon,such as ¹¹C, ¹³C and ¹⁴C, chlorine, such as ³⁶C1, fluorine, such as ¹⁸F,iodine, such as ¹²³I and ¹²⁵I, nitrogen, such as ¹³N and ¹⁵N, oxygen,such as ¹⁵O, ¹⁷O and ¹⁸O, phosphorus, such as ³²P, and sulphur, such as³⁵S.

Certain isotopically-labeled compounds of formula (I), for example,those incorporating a radioactive isotope, are useful in drug and/orsubstrate tissue distribution studies. The radioactive isotopes tritium,i.e. ³H, and carbon-14, i.e. ¹⁴C, are particularly useful for thispurpose in view of their ease of incorporation and ready means ofdetection.

Substitution with heavier isotopes such as deuterium, i.e. ²H, mayafford certain therapeutic advantages resulting from greater metabolicstability, for example, increased in vivo half-life or reduced dosagerequirements, and hence may be preferred in some circumstances.Substitution with positron emitting isotopes, such as ¹¹C, ¹⁸F, ¹⁵O and¹³N, can be useful in Positron Emission Topography (PET) studies forexamining substrate receptor occupancy.

Isotopically-labeled compounds of formula (I) can generally be preparedby conventional techniques known to those skilled in the art or byprocesses analogous to those described in the accompanying Examples andPreparations using an appropriate isotopically-labeled reagents in placeof the non-labeled reagent previously employed.

Pharmaceutically acceptable solvates in accordance with the inventioninclude those wherein the solvent of crystallization may be isotopicallysubstituted, e.g. D₂O, d₆-acetone, d₆-DMSO.

Compounds of the invention, i.e. compounds of formula (I) that containgroups capable of acting as donors and/or acceptors for hydrogen bondsmay be capable of forming co-crystals with suitable co-crystal formers.These co-crystals may be prepared from compounds of formula (I) by knownco-crystal forming procedures. Such procedures include grinding,heating, co-subliming, co-melting, or contacting in solution compoundsof formula (I) with the co-crystal former under crystallizationconditions and isolating co-crystals thereby formed. Suitable co-crystalformers include those described in WO 2004/078163. Hence the inventionfurther provides co-crystals comprising a compound of formula (I).

As used herein, the term “pharmaceutically acceptable carrier” includesany and all solvents, dispersion media, coatings, surfactants,antioxidants, preservatives (e.g., antibacterial agents, antifungalagents), isotonic agents, absorption delaying agents, salts,preservatives, drugs, drug stabilizers, binders, excipients,disintegration agents, lubricants, sweetening agents, flavoring agents,dyes, and the like and combinations thereof, as would be known to thoseskilled in the art (see, for example, Remington's PharmaceuticalSciences, 18th Ed. Mack Printing Company, 1990, pp. 1289-1329). Exceptinsofar as any conventional carrier is incompatible with the activeingredient, its use in the therapeutic or pharmaceutical compositions iscontemplated.

The term “a therapeutically effective amount” of a compound of thepresent invention refers to an amount of the compound of the presentinvention that will elicit the biological or medical response of asubject, for example, reduction or inhibition of an enzyme or a proteinactivity, or ameliorate symptoms, alleviate conditions, slow or delaydisease progression, or prevent a disease, etc. In one non-limitingembodiment, the term “a therapeutically effective amount” refers to theamount of the compound of the present invention that, when administeredto a subject, is effective to (1) at least partially alleviating,inhibiting, preventing and/or ameliorating a condition, or a disorder ora disease (i) mediated by NS3/NS4 serine protease activity; or (2)reducing or inhibiting the activity of NS3 serine protease; or (3)reducing or inhibiting replication of at least one virus which encodes aNS3 serine protease. In another non-limiting embodiment, the term “atherapeutically effective amount” refers to the amount of the compoundof the present invention that, when administered to a cell, or a tissue,or a non-cellular biological material, or a medium, is effective to atleast partially reducing or inhibiting viral load and/or viralreplication. The meaning of the term “a therapeutically effectiveamount” as illustrated in the above embodiment for NS3 protease alsoapplies by the same means to any other relevantproteins/peptides/enzymes, such as NS2 protease, the NS3 protease, theNS3 helicase, the NS5a protein, and/or the NS5b polymerase, and thelike.

As used herein, the term “subject” refers to an animal. Preferably, theanimal is a mammal. A subject also refers to for example, primates(e.g., humans), cows, sheep, goats, horses, dogs, cats, rabbits, rats,mice, fish, birds and the like. In a preferred embodiment, the subjectis a primate. In another preferred embodiment, the subject is a human.

As used herein, the term “inhibit”, “inhibition” or “inhibiting” refersto the reduction or suppression of a given condition, symptom, ordisorder, or disease, or a significant decrease in the baseline activityof a biological activity or process.

As used herein, the term “treat”, “treating” or “treatment” of anydisease or disorder refers in one embodiment, to ameliorating thedisease or disorder (i.e., slowing or arresting or reducing thedevelopment of the disease or at least one of the clinical symptomsthereof). In another embodiment “treat”, “treating” or “treatment”refers to alleviating or ameliorating at least one physical parameterincluding those which may not be discernible by the patient. In yetanother embodiment, “treat”, “treating” or “treatment” refers tomodulating the disease or disorder, either physically, (e.g.,stabilization of a discernible symptom), physiologically, (e.g.,stabilization of a physical parameter), or both. In yet anotherembodiment, “treat”, “treating” or “treatment” refers to preventing ordelaying the onset or development or progression of the disease ordisorder.

As used herein, a subject is “in need of” a treatment if such subjectwould benefit biologically, medically or in quality of life from suchtreatment.

As used herein, the term “a,” “an,” “the” and similar terms used in thecontext of the present invention (especially in the context of theclaims) are to be construed to cover both the singular and plural unlessotherwise indicated herein or clearly contradicted by the context.

All methods described herein can be performed in any suitable orderunless otherwise indicated herein or otherwise clearly contradicted bycontext. The use of any and all examples, or exemplary language (e.g.“such as”) provided herein is intended merely to better illuminate theinvention and does not pose a limitation on the scope of the inventionotherwise claimed.

Any asymmetric atom (e.g., carbon or the like) of the compound(s) of thepresent invention can be present in racemic or enantiomericallyenriched, for example the (R)-, (S)- or (R,S)-configuration. In certainembodiments, each asymmetric atom has at least 50% enantiomeric excess,at least 60% enantiomeric excess, at least 70% enantiomeric excess, atleast 80% enantiomeric excess, at least 90% enantiomeric excess, atleast 95% enantiomeric excess, or at least 99% enantiomeric excess inthe (R)- or (S)-configuration. Substituents at atoms with unsaturatedbonds may, if possible, be present in cis-(Z)- or trans-(E)-form.

Accordingly, as used herein a compound of the present invention can bein the form of one of the possible isomers, rotamers, atropisomers,tautomers or mixtures thereof, for example, as substantially puregeometric (cis or trans) isomers, diastereomers, optical isomers(antipodes), racemates or mixtures thereof.

Any resulting mixtures of isomers can be separated on the basis of thephysicochemical differences of the constituents, into the pure orsubstantially pure geometric or optical isomers, diastereomers,racemates, for example, by chromatography and/or fractionalcrystallization.

Any resulting racemates of final products or intermediates can beresolved into the optical antipodes by known methods, e.g., byseparation of the diastereomeric salts thereof, obtained with anoptically active acid or base, and liberating the optically activeacidic or basic compound. In particular, a basic moiety may thus beemployed to resolve the compounds of the present invention into theiroptical antipodes, e.g., by fractional crystallization of a salt formedwith an optically active acid, e.g., tartaric acid, dibenzoyl tartaricacid, diacetyl tartaric acid, di-O,O′-p-toluoyl tartaric acid, mandelicacid, malic acid or camphor-10-sulfonic acid. Racemic products can alsobe resolved by chiral chromatography, e.g., high pressure liquidchromatography (HPLC) using a chiral adsorbent.

Compounds of the present invention are either obtained in the free form,as a salt thereof, or as prodrug derivatives thereof.

When both a basic group and an acid group are present in the samemolecule, the compounds of the present invention may also form internalsalts, e.g., zwitterionic molecules.

The present invention also provides pro-drugs of the compounds of thepresent invention that converts in vivo to the compounds of the presentinvention. A pro-drug is an active or inactive compound that is modifiedchemically through in vivo physiological action, such as hydrolysis,metabolism and the like, into a compound of this invention followingadministration of the prodrug to a subject. The suitability andtechniques involved in making and using pro-drugs are well known bythose skilled in the art. Prodrugs can be conceptually divided into twonon-exclusive categories, bioprecursor prodrugs and carrier prodrugs.See The Practice of Medicinal Chemistry, Ch. 31-32 (Ed. Wermuth,Academic Press, San Diego, Calif., 2001). Generally, bioprecursorprodrugs are compounds, which are inactive or have low activity comparedto the corresponding active drug compound, that contain one or moreprotective groups and are converted to an active form by metabolism orsolvolysis. Both the active drug form and any released metabolicproducts should have acceptably low toxicity.

Carrier prodrugs are drug compounds that contain a transport moiety,e.g., that improve uptake and/or localized delivery to a site(s) ofaction. Desirably for such a carrier prodrug, the linkage between thedrug moiety and the transport moiety is a covalent bond, the prodrug isinactive or less active than the drug compound, and any releasedtransport moiety is acceptably non-toxic. For prodrugs where thetransport moiety is intended to enhance uptake, typically the release ofthe transport moiety should be rapid. In other cases, it is desirable toutilize a moiety that provides slow release, e.g., certain polymers orother moieties, such as cyclodextrins. Carrier prodrugs can, forexample, be used to improve one or more of the following properties:increased lipophilicity, increased duration of pharmacological effects,increased site-specificity, decreased toxicity and adverse reactions,and/or improvement in drug formulation (e.g., stability, watersolubility, suppression of an undesirable organoleptic or physiochemicalproperty). For example, lipophilicity can be increased by esterificationof (a) hydroxyl groups with lipophilic carboxylic acids (e.g., acarboxylic acid having at least one lipophilic moiety), or (b)carboxylic acid groups with lipophilic alcohols (e.g., an alcohol havingat least one lipophilic moiety, for example aliphatic alcohols).

Exemplary prodrugs are, e.g., esters of free carboxylic acids and S-acylderivatives of thiols and O-acyl derivatives of alcohols or phenols,wherein acyl has a meaning as defined herein. Preferred arepharmaceutically acceptable ester derivatives convertible by solvolysisunder physiological conditions to the parent carboxylic acid, e.g.,lower alkyl esters, cycloalkyl esters, lower alkenyl esters, benzylesters, mono- or di-substituted lower alkyl esters, such as the -(amino,mono- or di-lower alkylamino, carboxy, lower alkoxycarbonyl)-lower alkylesters, the -(lower alkanoyloxy, lower alkoxycarbonyl or di-loweralkylaminocarbonyl)-lower alkyl esters, such as the pivaloyloxymethylester and the like conventionally used in the art. In addition, amineshave been masked as arylcarbonyloxymethyl substituted derivatives whichare cleaved by esterases in vivo releasing the free drug andformaldehyde (Bundgaard, J. Med. Chem. 2503 (1989)). Moreover, drugscontaining an acidic NH group, such as imidazole, imide, indole and thelike, have been masked with N-acyloxymethyl groups (Bundgaard, Design ofProdrugs, Elsevier (1985)). Hydroxy groups have been masked as estersand ethers. EP 039,051 (Sloan and Little) discloses Mannich-basehydroxamic acid prodrugs, their preparation and use.

Furthermore, the compounds of the present invention, including theirsalts, can also be obtained in the form of their hydrates, or includeother solvents used for their crystallization.

In another aspect, the present invention provides a pharmaceuticalcomposition comprising a compound of the present invention and apharmaceutically acceptable carrier. The pharmaceutical composition canbe formulated for particular routes of administration such as oraladministration, parenteral administration, and rectal administration,etc. In addition, the pharmaceutical compositions of the presentinvention can be made up in a solid form including capsules, tablets,pills, granules, powders or suppositories, or in a liquid form includingsolutions, suspensions or emulsions. The pharmaceutical compositions canbe subjected to conventional pharmaceutical operations such assterilization and/or can contain conventional inert diluents,lubricating agents, or buffering agents, as well as adjuvants, such aspreservatives, stabilizers, wetting agents, emulsifers and buffers etc.

Typically, the pharmaceutical compositions are tablets and gelatincapsules comprising the active ingredient together with

a) diluents, e.g., lactose, dextrose, sucrose, mannitol, sorbitol,cellulose and/or glycine;

b) lubricants, e.g., silica, talcum, stearic acid, its magnesium orcalcium salt and/or polyethyleneglycol; for tablets also

c) binders, e.g., magnesium aluminum silicate, starch paste, gelatin,tragacanth, methylcellulose, sodium carboxymethylcellulose and/orpolyvinylpyrrolidone; if desired

d) disintegrants, e.g., starches, agar, alginic acid or its sodium salt,or effervescent mixtures; and/or

e) absorbents, colorants, flavors and sweeteners.

Tablets may be either film coated or enteric coated according to methodsknown in the art.

Suitable compositions for oral administration include an effectiveamount of a compound of the invention in the form of tablets, lozenges,aqueous or oily suspensions, dispersible powders or granules, emulsion,hard or soft capsules, or syrups or elixirs. Compositions intended fororal use are prepared according to any method known in the art for themanufacture of pharmaceutical compositions and such compositions cancontain one or more agents selected from the group consisting ofsweetening agents, flavoring agents, coloring agents and preservingagents in order to provide pharmaceutically elegant and palatablepreparations. Tablets contain the active ingredient in admixture withnontoxic pharmaceutically acceptable excipients which are suitable forthe manufacture of tablets. These excipients are, for example, inertdiluents, such as calcium carbonate, sodium carbonate, lactose, calciumphosphate or sodium phosphate; granulating and disintegrating agents,for example, corn starch, or alginic acid; binding agents, for example,starch, gelatin or acacia; and lubricating agents, for example magnesiumstearate, stearic acid or talc. The tablets are uncoated or coated byknown techniques to delay disintegration and absorption in thegastrointestinal tract and thereby provide a sustained action over alonger period. For example, a time delay material such as glycerylmonostearate or glyceryl distearate can be employed. Formulations fororal use can be presented as hard gelatin capsules wherein the activeingredient is mixed with an inert solid diluent, for example, calciumcarbonate, calcium phosphate or kaolin, or as soft gelatin capsuleswherein the active ingredient is mixed with water or an oil medium, forexample, peanut oil, liquid paraffin or olive oil.

Certain injectable compositions are aqueous isotonic solutions orsuspensions, and suppositories are advantageously prepared from fattyemulsions or suspensions. Said compositions may be sterilized and/orcontain adjuvants, such as preserving, stabilizing, wetting oremulsifying agents, solution promoters, salts for regulating the osmoticpressure and/or buffers. In addition, they may also contain othertherapeutically valuable substances. Said compositions are preparedaccording to conventional mixing, granulating or coating methods,respectively, and contain about 0.1-75%, or contain about 1-50%, of theactive ingredient.

Suitable compositions for transdermal application include an effectiveamount of a compound of the invention with carrier. Carriers includeabsorbable pharmacologically acceptable solvents to assist passagethrough the skin of the host. For example, transdermal devices are inthe form of a bandage comprising a backing member, a reservoircontaining the compound optionally with carriers, optionally a ratecontrolling barrier to deliver the compound of the skin of the host at acontrolled and predetermined rate over a prolonged period of time, andmeans to secure the device to the skin.

Suitable compositions for topical application, e.g., to the skin, eyesand mucas membranes, include aqueous solutions, suspensions, ointments,creams, gels or sprayable formulations, e.g., for delivery by aerosol orthe like. Such topical delivery systems will in particular beappropriate for vaginal application, e.g., for the prevention of HCVinfection. Such may contain solubilizers, stabilizers, tonicityenhancing agents, buffers and preservatives.

The present invention further provides anhydrous pharmaceuticalcompositions and dosage forms comprising the compounds of the presentinvention as active ingredients, since water may facilitate thedegradation of certain compounds.

Anhydrous pharmaceutical compositions and dosage forms of the inventioncan be prepared using anhydrous or low moisture containing ingredientsand low moisture or low humidity conditions. An anhydrous pharmaceuticalcomposition may be prepared and stored such that its anhydrous nature ismaintained. Accordingly, anhydrous compositions are preferably packagedusing materials known to prevent exposure to water such that they can beincluded in suitable formulary kits. Examples of suitable packaginginclude, but are not limited to, hermetically sealed foils, plastics,unit dose containers (e.g., vials), blister packs, and strip packs.

The invention further provides pharmaceutical compositions and dosageforms that comprise one or more agents that reduce the rate by which thecompound of the present invention as an active ingredient willdecompose. Such agents, which are referred to herein as “stabilizers,”include, but are not limited to, antioxidants such as ascorbic acid, pHbuffers, or salt buffers, etc.

The pharmaceutical composition or combination of the present inventioncan be in unit dosage of about 1-1000 mg of active ingredient(s) for asubject of about 50-70 kg, or about 1-500 mg or about 1-250 mg or about1-150 mg or about 0.5-100 mg, or about 1-50 mg of active ingredients.The therapeutically effective dosage of a compound, the pharmaceuticalcomposition, or the combinations thereof, is dependent on the species ofthe subject, the body weight, age and individual condition, the disorderor disease or the severity thereof being treated. A physician, clinicianor veterinarian of ordinary skill can readily determine the effectiveamount of each of the active ingredients necessary to prevent, treat orinhibit the progress of the disorder or disease.

The above-cited dosage properties are demonstrable in vitro and in vivotests using advantageously mammals, e.g., mice, rats, dogs, monkeys orisolated organs, tissues and preparations thereof. The compounds of thepresent invention can be applied in vitro in the form of solutions,e.g., preferably aqueous solutions, and in vivo either enterally,parenterally, advantageously intravenously, e.g., as a suspension or inaqueous solution. The dosage in vitro may range between about 10⁻³ molarand 10⁻⁹ molar concentrations. A therapeutically effective amount invivo may range depending on the route of administration, between about0.1-500 mg/kg, or between about 1-100 mg/kg.

The activity of a compound according to the present invention can beassessed by in vitro & in vivo methods including but not limited to themethods provided infra.

In one embodiment, the invention provides a pharmaceutical compositioncomprising a compound of formula (I) and another therapeutic agent(s).Optionally, the pharmaceutical composition may comprise apharmaceutically acceptable excipient, as described above.

In one embodiment, the invention provides a kit comprising two or moreseparate pharmaceutical compositions, at least one of which contains acompound of formula (I). In one embodiment, the kit comprises means forseparately retaining said compositions, such as a container, dividedbottle, or divided foil packet. An example of such a kit is a blisterpack, as typically used for the packaging of tablets, capsules and thelike.

The kit of the invention may be used for administering different dosageforms, for example, oral and parenteral, for administering the separatecompositions at different dosage intervals, or for titrating theseparate compositions against one another. To assist compliance, the kitof the invention typically comprises directions for administration.

In the combination therapies of the invention, the compound of theinvention and the other therapeutic agent may be manufactured and/orformulated by the same or different manufacturers. Moreover, thecompound of the invention and the other therapeutic may be broughttogether into a combination therapy: (i) prior to release of thecombination product to physicians (e.g. in the case of a kit comprisingthe compound of the invention and the other therapeutic agent); (ii) bythe physician themselves (or under the guidance of the physician)shortly before administration; (iii) in the patient themselves, e.g.during sequential administration of the compound of the invention andthe other therapeutic agent.

Accordingly, the invention provides the use of a compound of formula (I)for treating a disease or condition mediated by NS3 protease activity,including but not limited to viral infections selected from HCV, HIV andthe like, wherein the medicament is prepared for administration withanother therapeutic agent. The invention also provides the use ofanother therapeutic agent for treating a disease or condition mediatedby NS3 protease activity], wherein the medicament is administered with acompound of formula (I).

The invention also provides a compound of formula (I) for use in amethod of treating a disease or condition mediated by NS3 proteaseactivity, wherein the compound of formula (I) is prepared foradministration with another therapeutic agent. The invention alsoprovides another therapeutic agent for use in a method of treating adisease or condition mediated by NS3 protease activity, wherein theother therapeutic agent is prepared for administration with a compoundof formula (I). The invention also provides a compound of formula (I)for use in a method of treating a disease or condition mediated by NS3protease activity, wherein the compound of formula (I) is administeredwith another therapeutic agent. The invention also provides anothertherapeutic agent for use in a method of treating a disease or conditionmediated by NS3 protease activity, wherein the other therapeutic agentis administered with a compound of formula (I).

The invention also provides the use of a compound of formula (I) fortreating a viral infection, wherein the patient has previously (e.g.within 24 hours) been treated with another therapeutic agent. Theinvention also provides the use of another therapeutic agent fortreating a viral, wherein the patient has previously (e.g. within 24hours) been treated with a compound of formula (I).

In one embodiment, the other therapeutic agent is selected from:

A compound of the present invention may also be used in combination withother agents, e.g., an additional HCV-modulating compound that is or isnot of the formula I, for treatment of and HCV-associated disorder in asubject.

By the term “combination”, is meant either a fixed combination in onedosage unit form, or a kit of parts for the combined administrationwhere a compound of the present invention and a combination partner maybe administered independently at the same time or

separately within time intervals that especially allow that thecombination partners show a cooperative, e.g., synergistic, effect, orany combination thereof.

For example, WO 2005/042020, incorporated herein by reference in itsentirety, describes the combination of various HCV inhibitors with acytochrome P450 (“CYP”) inhibitor. Any CYP inhibitor that improves thepharmacokinetics of the relevant NS3/4A protease may be used incombination with the compounds of this invention. These CYP inhibitorsinclude, but are not limited to, ritonavir (WO 94/14436, incorporatedherein by reference in its entirety), ketoconazole, troleandomycin,4-methylpyrazole, cyclosporin, NIM811, clomethiazole, cimetidine,itraconazole, fluconazole, miconazole, fluvoxamine, fluoxetine,nefazodone, sertraline, indinavir, nelfinavir, amprenavir,fosamprenavir, saquinavir, lopinavir, delavirdine, erythromycin, VX-944,and VX-497. Preferred CYP inhibitors include ritonavir, ketoconazole,troleandomycin, 4-methylpyrazole, cyclosporin, NIM811, andclomethiazole.

Methods for measuring the ability of a compound to inhibit CYP activityare known (see, e.g., U.S. Pat. No. 6,037,157 and Yun, et al. DrugMetabolism & Disposition, vol. 21, pp. 403-407 (1993); incorporatedherein by reference). For example, a compound to be evaluated may beincubated with 0.1, 0.5, and 1.0 mg protein/ml, or other appropriateconcentration of human hepatic microsomes (e.g., commercially available,pooled characterized hepatic microsomes) for 0, 5, 10, 20, and 30minutes, or other appropriate times, in the presence of anNADPH-generating system. Control incubations may be performed in theabsence of hepatic microsomes for 0 and 30 minutes (triplicate). Thesamples may be analyzed for the presence of the compound. Incubationconditions that produce a linear rate of compound metabolism will beused a guide for further studies. Experiments known in the art can beused to determine the kinetics of the compound metabolism (K_(m) andV_(max)). The rate of disappearance of compound may be determined andthe data analyzed according to Michaelis-Menten kinetics by usingLineweaver-Burk, Eadie-Hofstee, or nonlinear regression analysis.

Inhibition of metabolism experiments may then be performed. For example,a compound (one concentration, <K_(m)) may be incubated with pooledhuman hepatic microsomes in the absence or presence of a CYP inhibitor(such as ritonavir) under the conditions determined above. As would berecognized, control incubations should contain the same concentration oforganic solvent as the incubations with the CYP inhibitor. Theconcentrations of the compound in the samples may be quantitated, andthe rate of

disappearance of parent compound may be determined, with rates beingexpressed as a percentage of control activity.

Methods for evaluating the influence of co-administration of a compoundof the invention and a CYP inhibitor in a subject are also known (see,e.g., US2004/0028755; incorporated herein by reference). Any suchmethods could be used in connection with this invention to determine thepharmacokinetic impact of a combination. Subjects that would benefitfrom treatment according to this invention could then be selected.

Accordingly, one embodiment of this invention provides a method foradministering an inhibitor of CYP3A4 and a compound of the invention.Another embodiment of this invention provides a method for administeringan inhibitor of isozyme 3A4 (“CYP3A4”), isozyme 2C19 (“CYP2C19”),isozyme 2D6 (“CYP2D6”), isozyme 1A2 (“CYP1A2”), isozyme 2C9 (“CYP2C9”),or isozyme 2E1 (“CYP2E1”). In embodiments where the protease inhibitoris VX-950 (or a sterereoisomer thereof), the CYP inhibitor preferablyinhibits CYP3A4.

As would be appreciated, CYP3A4 activity is broadly observed in humans.Accordingly, embodiments of this invention involving inhibition ofisozyme 3A4 would be expected to be applicable to a broad range ofpatients.

Accordingly, this invention provides methods wherein the CYP inhibitoris administered together with the compound of the invention in the samedosage form or in separate dosage forms.

The compounds of the invention (e.g., compound of Formula I orsubformulae thereof) may be administered as the sole ingredient or incombination or alteration with other antiviral agents, especially agentsactive against HCV. In combination therapy, effective dosages of two ormore agents are administered together, whereas in alternation orsequential-step therapy, an effective dosage of each agent isadministered serially or sequentially. In general, combination therapyis typically preferred over alternation therapy because it inducesmultiple simultaneous stresses on the virus. The dosages given willdepend on absorption, inactivation and excretion rate of the drug aswell as other factors. It is to be noted that dosage values will alsovary with the severity of the condition to be alleviated. It is to befurther understood that for any particular subject, specific dosageregimens and schedules should be adjusted over time according to theindividual need and the professional judgment of the personadministering or supervising the administration of the compositions. Theefficacy of a drug against the viral infection can be prolonged,augmented, or restored by administering the compound in combination oralternation with a second, and perhaps third antiviral compound thatinduces a different gene mutation than that caused by the principle drugin a drug resistant virus. Alternatively, the pharmacokinetic,biodistribution or other parameters of the drug can be altered by suchcombination or alternation therapy.

Daily dosages required in practicing the method of the present inventionwill vary depending upon, for example, the compound of the inventionemployed, the host, the mode of administration, the severity of thecondition to be treated. A preferred daily dosage range is about from 1to 50 mg/kg per day as a single dose or in divided doses. Suitable dailydosages for patients are on the order of from e.g. 1 to 20 mg/kg p.o ori.v. Suitable unit dosage forms for oral administration comprise fromca. 0.25 to 10 mg/kg active ingredient, e.g. compound of Formula I orany subformulae thereof, together with one or more pharmaceuticallyacceptable diluents or carriers therefor. The amount of co-agent in thedosage form can vary greatly, e.g., 0.00001 to 1000 mg/kg activeingredient.

Daily dosages with respect to the co-agent used will vary dependingupon, for example, the compound employed, the host, the mode ofadministration and the severity of the condition to be treated. Forexample, lamivudine may be administered at a daily dosage of 100 mg. Thepegylated interferon may be administered parenterally one to three timesper week, preferably once a week, at a total weekly dose ranging from 2to 10 million IU, more preferable 5 to 10 million IU, most preferable 8to 10 million IU. Because of the diverse types of co-agent that may beused, the amounts can vary greatly, e.g., 0.0001 to 5,000 mg/kg per day.

The current standard of care for treating hepatitis C is the combinationof pegylated interferon alpha with ribavirin, of which the recommendeddoses are 1.5 μg/kg/wk peginterferon alfa-2b or 180 g/wk peginterferonalfa-2a, plus 1,000 to 1,200 mg daily of ribavirin for 48 weeks forgenotype I patients, or 800 mg daily of ribavirin for 24 weeks forgenotype 2/3 patients.

The compound of the invention (e.g., compound of Formula I orsubformulae thereof) and co-agents of the invention may be administeredby any conventional route, in particular enterally, e.g. orally, forexample in the form of solutions for drinking, tablets or capsules orparenterally, for example in the form of injectable solutions orsuspensions. Certain preferred pharmaceutical compositions may be e.g.those based on microemulsions as described in UK 2,222,770 A.

The compound of the invention (e.g., compound of Formula I orsubformulae thereof) are administered together with other drugs(co-agents) e.g. a drug which has anti-viral activity, especiallyanti-Flaviviridae activity, most especially anti-HCV activity, e.g. aninterferon, e.g. interferon-α-2a or interferon-α-2b, e.g. Intron^(R) A,Roferon^(R), Avonex^(R), Rebif^(R) or Betaferon^(R), or an interferonconjugated to a water soluble polymer or to human albumin, e.g.albuferon, an anti-viral agent, e.g. ribavirin, lamivudine, thecompounds disclosed in U.S. Pat. No. 6,812,219 and WO 2004/002422 A2(the disclosures of which are incorporated herein by reference in theirentireties), an inhibitor of the HCV or other Flaviviridae virus encodedfactors like the NS3/4A protease, helicase or RNA polymerase or aprodrug of such an inhibitor, an anti-fibrotic agent, e.g. aN-phenyl-2-pyrimidine-amine derivative, e.g. imatinib, an immunemodulating agent, e.g. mycophenolic acid, a salt or a prodrug thereof,e.g. sodium mycophenolate or mycophenolate mofetil, or a S1P receptoragonist, e.g. FTY720 or an analogue thereof optionally phosphorylated,e.g. as disclosed in EP627406A1, EP778263A1, EP1002792A1, WO02/18395,WO02/76995, WO 02/06268, JP2002316985, WO03/29184, WO03/29205,WO03/62252 and WO03/62248, the disclosures of which are incorporatedherein by reference in their entireties.

Conjugates of interferon to a water-soluble polymer are meant to includeespecially conjugates to polyalkylene oxide homopolymers such aspolyethylene glycol (PEG) or polypropylene glycols, polyoxyethylenatedpolyols, copolymers thereof and block copolymers thereof. As analternative to polyalkylene oxide-based polymers, effectivelynon-antigenic materials such as dextran, polyvinyl pyrrolidones,polyacrylamides, polyvinyl alcohols, carbohydrate-based polymers and thelike can be used. Such interferon-polymer conjugates are described inU.S. Pat. Nos. 4,766,106, 4,917,888, European Patent Application No. 0236 987, European Patent Application No. 0 510 356 and InternationalApplication Publication No. WO 95/13090, the disclosures of which areincorporated herein by reference in their entireties. Since thepolymeric modification sufficiently reduces antigenic responses, theforeign interferon need not be completely autologous. Interferon used toprepare polymer conjugates may be prepared from a mammalian extract,such as human, ruminant or bovine interferon, or recombinantly produced.Preferred are conjugates of interferon to polyethylene glycol, alsoknown as pegylated interferons.

Especially preferred conjugates of interferon are pegylatedalfa-interferons, for example pegylated interferon-α-2a, pegylatedinterferon-α-2b; pegylated consensus interferon or pegylated purifiedinterferon-α product. Pegylated interferon-α-2a is described e.g. inEuropean Patent 593,868 (incorporated herein by reference in itsentirety) and commercially available e.g. under the tradename PEGASYS®(Hoffmann-La Roche). Pegylated interferon-α-2b is described, e.g. inEuropean Patent 975,369 (incorporated herein by reference in itsentirety) and commercially available e.g. under the tradename PEG-INTRONA® (Schering Plough). Pegylated consensus interferon is described in WO96/11953 (incorporated herein by reference in its entirety). Thepreferred pegylated α-interferons are pegylated interferon-α-2a andpegylated interferon-α-2b. Also preferred is pegylated consensusinterferon.

Other preferred co-agents are fusion proteins of an interferon, forexample fusion proteins of interferon-α-2a, interferon-α-2b; consensusinterferon or purified interferon-α product, each of which is fused withanother protein. Certain preferred fusion proteins comprise aninterferon (e.g., interferon-α-2b) and an albumin as described in U.S.Pat. No. 6,973,322 and international publications WO02/60071,WO05/003296 and WO05/077042 (Human Genome Sciences). A preferredinterferon conjugated to a human albumin is Albuferon (Human GenomeSciences).

Cyclosporins which bind strongly to cyclophilin but are notimmunosuppressive include those cyclosporins recited in U.S. Pat. Nos.5,767,069 and 5,981,479 and are incorporated herein by reference.Melle⁴-Cyclosporin (i.e., NIM811) and Debio-025 (Debiopharm) arepreferred non-immunosuppressive cyclosporins. Certain other cyclosporinderivatives are described in WO2006039668 (Scynexis) and WO2006038088(Debiopharm SA) and are incorporated herein by reference. A cyclosporinis considered to be non-immunosuppressive when it has an activity in theMixed Lymphocyte Reaction (MLR) of no more than 5%, preferably no morethan 2%, that of cyclosporin A. The Mixed Lymphocyte Reaction isdescribed by T. Meo in “Immunological Methods”, L. Lefkovits and B.Peris, Eds., Academic Press, N.Y. pp. 227-239 (1979). Spleen cells(0.5×10⁶) from Balb/c mice (female, 8-10 weeks) are co-incubated for 5days with 0.5×10⁶ irradiated (2000 rads) or mitomycin C treated spleencells from CBA mice (female, 8-10 weeks). The irradiated allogeneiccells induce a proliferative response in the Balb c spleen cells whichcan be measured by labeled precursor incorporation into the DNA. Sincethe stimulator cells are irradiated (or mitomycin C treated) they do notrespond to the Balb/c cells with proliferation but do retain theirantigenicity. The IC₅₀ found for the test compound in the MLR iscompared with that found for cyclosporin A in a parallel experiment. Inaddition, non-immunosuppressive cyclosporins lack the capacity ofinhibiting CN and the downstream NF-AT pathway. [Melle]⁴-ciclosporin isa preferred non-immunosuppressive cyclophilin-binding cyclosporin foruse according to the invention.

Ribavirin (1-β-D-ribofuranosyl-1-1,2,4-triazole-3-caroxamide) is asynthetic, non-interferon-inducing, broad spectrum antiviral nucleosideanalog sold under the trade name, Virazole (The Merck Index, 11^(th)edition, Editor: Budavar, S, Merck & Co., Inc., Rahway, N.J., p 1304,1989). U.S. Pat. No. 3,798,209 and RE29,835 (incorporated herein byreference in their entireties) disclose and claim ribavirin. Ribavirinis structurally similar to guanosine, and has in vitro activity againstseveral DNA and RNA viruses including Flaviviridae (Gary L. Davis,Gastroenterology 118:S104-S114, 2000).

Ribavirin reduces serum amino transferase levels to normal in 40% ofpatients, but it does not lower serum levels of HCV-RNA (Gary L. Davis,Gastroenterology 118:S104-S114, 2000). Thus, ribavirin alone is noteffective in reducing viral RNA levels. Additionally, ribavirin hassignificant toxicity and is known to induce anemia. Ribavirin is notapproved for monotherapy against HCV; it is approved in combination withinterferon alpha-2a or interferon alpha-2b for the treatment of HCV.

A further preferred combination is a combination of a compound of theinvention (e.g., a compound of Formula I or any subformulae thereof)with a non-immunosuppressive cyclophilin-binding cyclosporine, withmycophenolic acid, a salt or a prodrug thereof, and/or with a S1Preceptor agonist, e.g. FTY720.

Additional examples of compounds that can be used in combination oralternation treatments include:

(1) Interferons, including interferon alpha 2a or 2b and pegylated (PEG)interferon alpha 2a or 2b, for example:

(a) Intron-A®, interferon alfa-2b (Schering Corporation, Kenilworth,N.J.);

(b) PEG-Intron®, peginteferon alfa-2b (Schering Corporation, Kenilworth,N.J.);

(c) Roferon®, recombinant interferon alfa-2a (Hoffmann-La Roche, Nutley,N.J.);

(d) Pegasys®, peginterferon alfa-2a (Hoffmann-La Roche, Nutley, N.J.);

(e) Berefor®, interferon alfa 2 available (Boehringer IngelheimPharmaceutical, Inc., Ridgefield, Conn.);

(f) Sumiferon®, a purified blend of natural alpha interferons (Sumitomo,Japan)

(g) Wellferon®, lymphoblastoid interferon alpha n1 (GlaxoSmithKline);

(h) Infergen®, consensus alpha interferon (InterMune Pharmaceuticals,Inc., Brisbane, Calif.);

(i) Alferon®, a mixture of natural alpha interferons (InterferonSciences, and Purdue Frederick Co., CT);

(j) Viraferon®;

(k) Consensus alpha interferon from Amgen, Inc., Newbury Park, Calif.,

Other forms of interferon include: interferon beta, gamma, tau andomega, such as Rebif (Interferon beta 1a) by Serono, Omniferon (naturalinterferon) by Viragen, REBIF (interferon beta-1a) by Ares-Serono, OmegaInterferon by BioMedicines; oral Interferon Alpha by AmarilloBiosciences; an interferon conjugated to a water soluble polymer or to ahuman albumin, e.g., Albuferon (Human Genome Sciences), an antiviralagent, a consensus interferon, ovine or bovine interferon-tau

Conjugates of interferon to a water-soluble polymer are meant to includeespecially conjugates to polyalkylene oxide homopolymers such aspolyethylene glocol (PEG) or polypropylene glycols, polyoxyethylenatedpolyols, copolymers thereof and block copolymers thereof. As analternative to polyalkylene oxid-based polymers, effectivelynon-antigenic materials such as dextran, polyvinyl pyrrolidones,polyacrylamides, polyvinyl alcohols, carbohydrate-based polymers and thelike can be used. Since the polymeric modification sufficiently reducesantigenic response, the foreign interferon need not be completelyautologous. Interferon used to prepare polymer conjugates may beprepared from a mammalian extract, such as human, ruminant or bovineinterferon, or recombinantly produced. Preferred are conjugates ofinterferon to polyethylene glycol, also known as pegylated interferons.

(2) Ribavirin, such as ribavirin(1-beta-D-ribofuranosyl-1H-1,2,4-triazole-3-carboxamide) from ValeantPharmaceuticals, Inc., Costa Mesa, Calif.); Rebetol® from ScheringCorporation, Kenilworth, N.J., and Copegus® from Hoffmann-La Roche,Nutley, N.J.; and new ribavirin analogues in development such asLevovirin and Viramidine by Valeant,

(3) Thiazolidine derivatives which show relevant inhibition in areverse-phase HPLC assay with an NS3/4A fusion protein and NS5A/5Bsubstrate (Sudo K. et al., Antiviral Research, 1996, 32, 9-18),especially compound RD-1-6250, possessing a fused cinnamoyl moietysubstituted with a long alkyl chain, RD4 6205 and RD4 6193;

(4) Thiazolidines and benzanilides identified in Kakiuchi N. et al. J.FEBS Letters 421, 217-220; Takeshita N. et al. Analytical Biochemistry,1997, 247, 242-246;

(5) A phenan-threnequinone possessing activity against protease in aSDS-PAGE and autoradiography assay isolated from the fermentationculture broth of Streptomyces sp., Sch 68631 (Chu M. et al., TetrahedronLetters, 1996, 37, 7229-7232), and Sch 351633, isolated from the fungusPenicillium griseofulvum, which demonstrates activity in a scintillationproximity assay (Chu M. et al, Bioorganic and Medicinal ChemistryLetters 9, 1949-1952);

(6) Protease inhibitors.

Examples include substrate-based NS3 protease inhibitors (Attwood etal., Antiviral peptide derivatives, PCT WO 98/22496, 1998; Attwood etal., Antiviral Chemistry and Chemotherapy 1999, 10, 259-273; Attwood etal, Preparation and use of amino acid derivatives as anti-viral agents,German Patent Pub. DE 19914474; Tung et al. Inhibitors of serineproteases, particularly hepatitis C virus NS3 protease; PCT WO98/17679), including alphaketoamides and hydrazinoureas, and inhibitorsthat terminate in an electrophile such as a boronic acid or phosphonate(Llinas-Brunet et al. Hepatitis C inhibitor peptide analogues, PCT WO99/07734) are being investigated.

Non-substrate-based NS3 protease inhibitors such as2,4,6-trihydroxy-3-nitro-benzamide derivatives (Sudo K. et al.,Biochemical and Biophysical Research Communications, 1997, 238 643-647;Sudo K. et al. Antiviral Chemistry and Chemotherapy, 1998, 9, 186),including RD3-4082 and RD3-4078, the former substituted on the amidewith a 14 carbon chain and the latter processing a para-phenoxyphenylgroup are also being investigated.

Sch 68631, a phenanthrenequinone, is an HCV protease inhibitor (Chu M etal., Tetrahedron Letters 37:7229-7232, 1996). In another example by thesame authors, Sch 351633, isolated from the fungus Penicilliumgrieofulvum, was identified as a protease inhibitor (Chu M. et al.,Bioorganic and Medicinal Chemistry Letters 9:1949-1952). Nanomolarpotency against the HCV NS3 protease enzyme has been achieved by thedesign of selective inhibitors based on the macromolecule eglin c. Eglinc, isolated from leech, is a potent inhibitor of several serineproteases such as S. griseus proteases A and B, α-chymotrypsin, chymaseand subtilisin. Qasim M. A. et al., Biochemistry 36:1598-1607, 1997.

U.S. patents disclosing protease inhibitors for the treatment of HCVinclude, for example, U.S. Pat. No. 6,004,933 to Spruce et al(incorporated herein by reference in its entirety) which discloses aclass of cysteine protease inhibitors for inhibiting HCV endopeptidase2; U.S. Pat. No. 5,990,276 to Zhang et al. (incorporated herein byreference in its entirety) which discloses synthetic inhibitors ofhepatitis C virus NS3 protease; U.S. Pat. No. 5,538,865 to Reyes et al.(incorporated herein by reference in its entirety). Peptides as NS3serine protease inhibitors of HCV are disclosed in WO 02/008251 toCorvas International, Inc., and WO 02/08187 and WO 02/008256 to ScheringCorporation (incorporated herein by reference in their entireties). HCVinhibitor tripeptides are disclosed in U.S. Pat. Nos. 6,534,523,6,410,531 and 6,420,380 to Boehringer Ingelheim and WO 02/060926 toBristol Myers Squibb (incorporated herein by reference in theirentireties). Diaryl peptides as NS3 serine protease inhibitors of HCVare disclosed in WO 02/48172 to Schering Corporation (incorporatedherein by reference). Imidazoleidinones as NS3 serine proteaseinhibitors of HCV are disclosed in WO 02/18198 to Schering Corporationand WO 02/48157 to Bristol Myers Squibb (incorporated herein byreference in their entireties). WO 98/17679 to Vertex Pharmaceuticalsand WO 02/48116 to Bristol Myers Squibb also disclose HCV proteaseinhibitors (incorporated herein by reference in their entireties).

HCV NS3-4A serine protease inhibitors including BILN 2061 by BoehringerIngelheim, VX-950 by Vertex, SCH 6/7 by Schering-Plough, TMC-435350(Tibotec/Johnson&Johnson) and other compounds currently in preclinicaldevelopment;

Substrate-based NS3 protease inhibitors, including alphaketoamides andhydrazinoureas, and inhibitors that terminate in an elecrophile such asa boronic acid or phosphonate; Non-substrate-based NS3 proteaseinhibitors such as 2,4,6-trihydroxy-3-nitro-benzamide derivativesincluding RD3-4082 and RD3-4078, the former substituted on the amidewith a 14 carbon chain and the latter processing a para-phenoxyphenylgroup; and Sch68631, a phenanthrenequinone, an HCV protease inhibitor.

Sch 351633, isolated from the fungus Penicillium griseofulvum wasidentified as a protease inhibitor. Eglin c, isolated from leech is apotent inhibitor of several serine proteases such as S. griseusproteases A and B, α-chymotrypsin, chymase and subtilisin.

U.S. Pat. No. 6,004,933 (incorporated herein by reference in itsentirety) discloses a class of cysteine protease inhibitors frominhibiting HCV endopeptidase 2; synthetic inhibitors of HCV NS3 protease(pat), HCV inhibitor tripeptides (pat), diaryl peptides such as NS3serine protease inhibitors of HCV (pat), Imidazolidindiones as NS3serine protease inhibitors of HCV (pat).

Thiazolidines and benzanilides (ref). Thiazolidine derivatives whichshow relevant inhibition in a reverse-phase HPLC assay with an NS3/4Afusion protein and NS5A/5B substrate especially compound RD-16250possessing a fused cinnamoyl moiety substituted with a long alkyl chain,RD4 6205 and RD4 6193.

HCV NS5A inhibitors including BMS-790052 by Bristol-Myers Squibb andother compounds currently in preclinical development.

Phenan-threnequinone possessing activity against protease in a SDS-PAGEand autoradiography assay isolated from the fermentation culture brothof Streptomyces sp, Sch68631 and Sch351633, isolated from the fungusPenicillium griseofulvum, which demonstrates activity in a scintillationproximity assay.

(7) Nucleoside or non-nucleoside inhibitors of HCV NS5B RNA-dependentRNA polymerase, such as 2′-C-methyl-3′-O-L-valine ester ribofuranosylcytidine (Idenix) as disclosed in WO 2004/002422 A2 (incorporated hereinby reference in its entirety), R803 (Rigel), JTK-003 (Japan Tabacco),HCV-086 (ViroPharma/Wyeth) and other compounds currently in preclinicaldevelopment;

gliotoxin (ref) and the natural product cerulenin;

2′-fluoronucleosides;

other nucleoside analogues as disclosed in WO 02/057287 A2, WO 02/057425A2, WO 01/90121, WO 01/92282, and U.S. Pat. No. 6,812,219, thedisclosures of which are incorporated herein by reference in theirentirety.

Idenix Pharmaceuticals discloses the use of branched nucleosides in thetreatment of flaviviruses (including HCV) and pestiviruses inInternational Publication Nos. WO 01/90121 and WO 01/92282 (incorporatedherein by reference in their entireties). Specifically, a method for thetreatment of hepatitis C infection (and flaviviruses and pestiviruses)in humans and other host animals is disclosed in the Idenix publicationsthat includes administering an effective amount of a biologically active1′, 2′, 3′ or 4′-branched B-D or B-L nucleosides or a pharmaceuticallyacceptable salt or prodrug thereof, administered either alone or incombination with another antiviral agent, optionally in apharmaceutically acceptable carrier. Certain preferred biologicallyactive 1′, 2′, 3′, or 4′ branched B-D or B-L nucleosides, includingTelbivudine, are described in U.S. Pat. Nos. 6,395,716 and 6,875,751,each of which are incorporated herein by reference.

Other patent applications disclosing the use of certain nucleosideanalogs to treat hepatitis C virus include: PCTCA00/01316 (WO 01/32153;filed Nov. 3, 2000) and PCT/CA01/00197 (WO 01/60315; filed Feb. 19,2001) filed by BioChem Pharma, Inc., (now Shire Biochem, Inc.);PCT/US02/01531 (WO 02/057425; filed Jan. 18, 2002) and PCT/US02/03086(WO 02/057287; filed Jan. 18, 2002) filed by Merck & Co., Inc.,PCT/EP01/09633 (WO 02/18404; published Aug. 21, 2001) filed by Roche,and PCT Publication Nos. WO 01/79246 (filed Apr. 13, 2001), WO 02/32920(filed Oct. 18, 2001) and WO 02/48165 by Pharmasset, Ltd. (thedisclosures of which are incorporated herein by reference in theirentireties)

PCT Publication No. WO 99/43691 to Emory University (incorporated hereinby reference in its entirety), entitled “2′-Fluoronucleosides” disclosesthe use of certain 2′-fluoronucleosides to treat HCV.

Eldrup et al. (Oral Session V, Hepatitis C Virus, Flaviviridae; 16^(th)International Conference on Antiviral Research (Apr. 27, 2003, Savannah,Ga.)) described the structure activity relationship of 2′-modifiednucleosides for inhibition of HCV.

Bhat et al. (Oral Session V, Hepatitis C Virus, Flaviviridae, 2003 (OralSession V, Hepatitis C Virus, Flaviviridae; 16^(th) Internationalconference on Antiviral Research (Apr. 27, 2003, Savannah, Ga.); p A75)describes the synthesis and pharmacokinetic properties of nucleosideanalogues as possible inhibitors of HCV RNA replication. The authorsreport that 2′-modified nucleosides demonstrate potent inhibitoryactivity in cell-based replicon assays.

Olsen et al. (Oral Session V, Hepatitis C Virus, Flaviviridae; 16^(th)International Conference on Antiviral Research (Apr. 27, 2003, Savannah,Ga.) p A76) also described the effects of the 2′-modified nucleosides onHCV RNA replication.

(8) Nucleotide polymerase inhibitors and gliotoxin (Ferrari R. et al.Journal of Virology, 1999, 73, 1649-1654), and the natural productcerulenin (Lohmann V. et al. Virology, 1998, 249, 108-118);

(9) HCV NS3 helicase inhibitors, such as VP_(—)50406 by ViroPhama andcompounds from Vertex. Other helicase inhibitors (Diana G. D. et al.,Compounds, compositions and methods for treatment of hepatitis C, U.S.Pat. No. 5,633,358 (incorporated herein by reference in its entirety);Diana G. D. et al., Piperidine derivatives, pharmaceutical compositionsthereof and their use in the treatment of hepatitis C, PCT WO 97/36554);

(10) Antisense phosphorothioate oligodeoxynucleotides (S-ODN)complementary to sequence stretches in the 5′ non-coding region (NCR) ofthe virus (Alt M. et al., Hepatology, 1995, 22, 707-717), or nucleotides326-348 comprising the 3′ end of the NCR and nucleotides 371-388 locatedin the core coding region of the HCV RNA (Alt M. et al., Archives ofVirology, 1997, 142, 589-599; Galderisi U. et al., Journal of CellularPhysiology, 199, 181, 251-257); such as ISIS 14803 by Isis Pharm/Elan,antisense by Hybridon, antisense by AVI bioPharma,

(11) Inhibitors of IRES-dependent translation (Ikeda N et al., Agent forthe prevention and treatment of hepatitis C, Japanese Patent Pub.JP-08268890; Kai Y et al. Prevention and treatment of viral diseases,Japanese Patent Pub. JP-10101591); such as ISIS 14803 by IsisPharm/Elan, IRES inhibitor by Anadys, IRES inhibitors by Immusol,targeted RNA chemistry by PTC Therapeutics

(12) Ribozymes, such as nuclease-resistant ribozymes (Maccjak, D. J. etal., Hepatology 1999, 30, abstract 995) and those directed in U.S. Pat.No. 6,043,077 to Barber et al., and U.S. Pat. Nos. 5,869,253 and5,610,054 to Draper et al. (incorporated herein by reference in theirentireties) for example, HEPTAZYME by RPI

(13) siRNA directed against HCV genome

(14) HCV replication inhibitor of any other mechanisms such as byVP50406ViroPharama/Wyeth, inhibitors from Achillion, Arrow

(15) An inhibitor of other targets in the HCV life cycle including viralentry, assembly and maturation

(16) An immune modulating agent such as an IMPDH inhibitor, mycophenolicacid, a salt or a prodrug thereof sodium mycophenolate or mycophenolatemofetil, or Merimebodib (VX-497); thymosin alpha-1 (Zadaxin, bySciClone); or a S1P receptor agonist, e.g. FTY720 or analogue thereofoptionally phosphorylated.

(17) An anti-fibrotic agent, such as a N-phenyl-2-pyrimidine-aminederivative, imatinib (Gleevac), IP-501 by Indevus, and Interferon gamma1b from InterMune

(18) Therapeutic vaccine by Intercell, Epimmune/Genecor, Merix, Tripep(Chron-VacC), immunotherapy (Therapore) by Avant, T cell therapy byCellExSys, monoclonal antibody XTL-002 by STL, ANA 246 and ANA 246 BYAnadys,

(19) Other miscellaneous compounds including 1-amino-alkylcyclohexanes(U.S. Pat. No. 6,034,134 to Gold et al.), alkyl lipids (U.S. Pat. No.5,922,757 to Chojkier et al.), vitamin E and other anti-oxidants (U.S.Pat. No. 5,922,757 to Chojkier et al.), amantadine, bile acids (U.S.Pat. No. 5,846,99964 to Ozeki et al.), N-(phosphonoacetyl)-L-asparticacid) U.S. Pat. No. 5,830,905 to Diana et al.), benzenedicarboxamides(U.S. Pat. No. 5,633,388 to Diane et al.), polyadenylic acid derivatives(U.S. Pat. No. 5,496,546 to Wang et al.), 2′3′-dideoxyinosine (U.S. Pat.No. 5,026,687 to Yarchoan et al.), benzimidazoles (U.S. Pat. No.5,891,874 to Colacino et al.), plant extracts (U.S. Pat. No. 5,837,257to Tsai et al., U.S. Pat. No. 5,725,859 to Omer et al., and U.S. Pat.No. 6,056,961) and piperidines (U.S. Pat. No. 5,830,905 to Diana etal.); the disclosures of which are incorporated herein by reference intheir entireties. Also, squalene, telbivudine,N-(phosphonoacetyl)-L-aspartic acid, benzenedicarboxamides, polyadenylicacid derivatives, glycosylation inhibitors, and nonspecificcytoprotective agents that block cell injury caused by the virusinfection.

(20) Any other compound currently in preclinical or clinical developmentfor the treatment of HCV, including Interleukin-10 (Schering-Plough),AMANTADINE (Symmetrel) by Endo Labs Solvay, caspase inhibitor IDN-6556by Idun Pharma, HCV/MF59 by Chiron, CIVACIR (Hepatitis C ImmuneGlobulin) by NABI, CEPLENE (histamine dichloride) by Maxim, IDN-6556 byIdun PHARM, T67, a beta-tubulin inhibitor, by Tularik, a therapeuticvaccine directed to E2 by Innogenetics, FK788 by Fujisawa Helathcare,IdB1016 (Siliphos, oral silybin-phosphatidyl choline phytosome), fusioninhibitor by Trimeris, Dication by Immtech, hemopurifier by AethlonMedical, UT 231B by United Therapeutics.

(21) Purine nucleoside analog antagonists of TlR7 (toll-like receptors)developed by Anadys, e.g., Isotorabine (ANA245) and its prodrug(ANA975), which are described in European applications EP348446 andEP636372, International Publications WO03/045968, WO05/121162 andWO05/25583, and U.S. Pat. No. 6,973,322, each of which is incorporatedby reference.

(22) Non-nucleoside inhibitors developed by Genelabs and described inInternational Publications WO2004/108687, WO2005/12288, andWO2006/076529, each of which is incorporated by reference.

(23) Other co-agents (e.g., non-immunomodulatory or immunomodulatorycompounds) that may be used in combination with a compound of thisinvention include, but are not limited to, those specified in WO02/18369 and WO2008021927A2 (e.g., BMS-790052), the structures of saidcompounds are incorporated herein by reference.

Methods of this invention may also involve administration of anothercomponent comprising an additional agent selected from animmunomodulatory agent; an antiviral agent; an inhibitor of HCVprotease; an inhibitor of another target in the HCV life cycle; a CYPinhibitor; or combinations thereof.

Accordingly, in another embodiment, this invention provides a methodcomprising administering a compound of the invention and anotheranti-viral agent, preferably an anti-HCV agent. Such anti-viral agentsinclude, but are not limited to, immunomodulatory agents, such as α, β,and δ interferons, pegylated derivatized interferon-a compounds, andthymosin; other anti-viral agents, such as ribavirin, amantadine, andtelbivudine; other inhibitors of hepatitis C proteases (NS2-NS3inhibitors and NS3-NS4A inhibitors); inhibitors of other targets in theHCV life cycle, including helicase, polymerase, and metalloproteaseinhibitors; inhibitors of internal ribosome entry; broad-spectrum viralinhibitors, such as IMPDH inhibitors (e.g., compounds of U.S. Pat. Nos.5,807,876, 6,498,178, 6,344,465, 6,054,472, WO 97/40028, WO 98/40381, WO00/56331, and mycophenolic acid and derivatives thereof, and including,but not limited to VX-497, VX-148, and/or VX-944); or combinations ofany of the above.

In accordance with the foregoing the present invention provides in a yetfurther aspect(s):

-   -   A pharmaceutical combination comprising a) a first agent which        is a compound of the invention, e.g. a compound of formula I or        any subformulae thereof, and b) a co-agent, e.g. a second drug        agent as defined above.    -   A method as defined above comprising co-administration, e.g.        concomitantly or in sequence, of a therapeutically effective        amount of a compound of the invention, e.g. a compound of        formula I or any subformulae thereof, and a co-agent, e.g. a        second drug agent as defined above.

The terms “co-administration” or “combined administration” or the likeas utilized herein are meant to encompass administration of the selectedtherapeutic agents to a single patient, and are intended to includetreatment regimens in which the agents are not necessarily administeredby the same route of administration or at the same time. Fixedcombinations are also within the scope of the present invention. Theadministration of a pharmaceutical combination of the invention resultsin a beneficial effect, e.g. a synergistic therapeutic effect, comparedto a monotherapy applying only one of its pharmaceutically activeingredients.

Each component of a combination according to this invention may beadministered separately, together, or in any combination thereof. Asrecognized by skilled practitioners, dosages of interferon are typicallymeasured in IU (e.g., about 4 million IU to about 12 million IU).

If an additional agent is selected from another CYP inhibitor, themethod would, therefore, employ two or more CYP inhibitors. Eachcomponent may be administered in one or more dosage forms. Each dosageform may be administered to the patient in any order.

The compound of the invention and any additional agent may be formulatedin separate dosage forms. Alternatively, to decrease the number ofdosage forms administered to a patient, the compound of the inventionand any additional agent may be formulated together in any combination.For example, the compound of the invention inhibitor may be formulatedin one dosage form and the additional agent may be formulated togetherin another dosage form. Any separate dosage forms may be administered atthe same time or different times.

Alternatively, a composition of this invention comprises an additionalagent as described herein. Each component may be present in individualcompositions, combination compositions, or in a single composition.

Use in HCV-Associated Disorders

The compounds of the present invention have valuable pharmacologicalproperties and are useful in the treatment of diseases. In certainembodiments, compounds of the invention are useful in the treatment ofHCV-associated disorders, e.g., as drugs to treat HCV infection.

The term “use” includes any one or more of the following embodiments ofthe invention, respectively: the use in the treatment of HCV-associateddisorders; the use for the manufacture of pharmaceutical compositionsfor use in the treatment of these diseases, e.g., in the manufacture ofa medicament; methods of use of compounds of the invention in thetreatment of these diseases; pharmaceutical preparations havingcompounds of the invention for the treatment of these diseases; andcompounds of the invention for use in the treatment of these diseases;as appropriate and expedient, if not stated otherwise. In particular,diseases to be treated and are thus preferred for use of a compound ofthe present invention are selected from HCV-associated disorders,including those corresponding to HCV-infection, as well as thosediseases that depend on the activity of one or more of the NS3, NS4A,NS4B, NS5A and NS5B proteins, or a NS3-NS4A, NS4A-NS4B, NS4B-NS5A orNS5A-NS5B complex. The term “use” further includes embodiments ofcompositions herein which bind to an HCV protein sufficiently to serveas tracers or labels, so that when coupled to a fluor or tag, or maderadioactive, can be used as a research reagent or as a diagnostic or animaging agent.

In certain embodiments, a compound of the present invention is used fortreating HCV-associated diseases, and use of the compound of the presentinvention as an inhibitor of any one or more HCVs. It is envisioned thata use can be a treatment of inhibiting one or more strains of HCV.

Assays

The inhibition of HCV activity may be measured as using a number ofassays available in the art. An example of such an assay can be found inAnal Biochem. 1996 240(1): 60-7; which is incorporated by reference inits entirety. Assays for measurement of HCV activity are also describedin the experimental section below.

Synthetic Procedure

Compounds of the present invention are prepared from commonly availablecompounds using procedures known to those skilled in the art, includingany one or more of the following conditions without limitation:

Within the scope of this text, only a readily removable group that isnot a constituent of the particular desired end product of the compoundsof the present invention is designated a “protecting group,” unless thecontext indicates otherwise. The protection of functional groups by suchprotecting groups, the protecting groups themselves, and their cleavagereactions are described for example in standard reference works, such ase.g., Science of Synthesis: Houben-Weyl Methods of MolecularTransformation. Georg Thieme Verlag, Stuttgart, Germany. 2005. 41627 pp.(URL: http://www.science-of-synthesis.com (Electronic Version, 48Volumes)); J. F. W. McOmie, “Protective Groups in Organic Chemistry”,Plenum Press, London and New York 1973, in T. W. Greene and P. G. M.Wuts, “Protective Groups in Organic Synthesis”, Third edition, Wiley,New York 1999, in “The Peptides”; Volume 3 (editors: E. Gross and J.Meienhofer), Academic Press, London and New York 1981, in “Methoden derorganischen Chemie” (Methods of Organic Chemistry), Houben Weyl, 4thedition, Volume 15/I, Georg Thieme Verlag, Stuttgart 1974, in H.-D.Jakubke and H. Jeschkeit, “Aminosäuren, Peptide, Proteine” (Amino acids,Peptides, Proteins), Verlag Chemie, Weinheim, Deerfield Beach, and Basel1982, and in Jochen Lehmann, “Chemie der Kohlenhydrate: Monosaccharideund Derivate” (Chemistry of Carbohydrates: Monosaccharides andDerivatives), Georg Thieme Verlag, Stuttgart 1974. A characteristic ofprotecting groups is that they can be removed readily (i.e., without theoccurrence of undesired secondary reactions) for example by solvolysis,reduction, photolysis or alternatively under physiological conditions(e.g., by enzymatic cleavage).

Mixtures of isomers obtainable according to the invention can beseparated in a manner known per se into the individual isomers;diastereoisomers can be separated, for example, by partitioning betweenpolyphasic solvent mixtures, recrystallisation and/or chromatographicseparation, for example over silica gel or by, e.g., medium pressureliquid chromatography over a reversed phase column, and racemates can beseparated, for example, by the formation of salts with optically puresalt-forming reagents and separation of the mixture of diastereoisomersso obtainable, for example by means of fractional crystallisation, or bychromatography over optically active column materials.

Intermediates and final products can be worked up and/or purifiedaccording to standard methods, e.g., using chromatographic methods,distribution methods, (re-) crystallization, and the like.

General Process Conditions

The following applies in general to all processes mentioned throughoutthis disclosure.

The process steps to synthesize the compounds of the invention can becarried out under reaction conditions that are known per se, includingthose mentioned specifically, in the absence or, customarily, in thepresence of solvents or diluents, including, for example, solvents ordiluents that are inert towards the reagents used and dissolve them, inthe absence or presence of catalysts, condensation or neutralizingagents, for example ion exchangers, such as cation exchangers, e.g., inthe H⁺ form, depending on the nature of the reaction and/or of thereactants at reduced, normal or elevated temperature, for example in atemperature range of from about −100° C. to about 190° C., including,for example, from approximately −80° C. to approximately 150° C., forexample at from −80 to −60° C., at room temperature, at from −20 to 40°C. or at reflux temperature, under atmospheric pressure or in a closedvessel, where appropriate under pressure, and/or in an inert atmosphere,for example under an argon or nitrogen atmosphere.

At all stages of the reactions, mixtures of isomers that are formed canbe separated into the individual isomers, for example diastereoisomersor enantiomers, or into any desired mixtures of isomers, for exampleracemates or mixtures of diastereoisomers, for example analogously tothe methods described in Science of Synthesis: Houben-Weyl Methods ofMolecular Transformation. Georg Thieme Verlag, Stuttgart, Germany. 2005.

The solvents from which those solvents that are suitable for anyparticular reaction may be selected include those mentioned specificallyor, for example, water, esters, such as lower alkyl-lower alkanoates,for example ethyl acetate, ethers, such as aliphatic ethers, for examplediethyl ether, or cyclic ethers, for example tetrahydrofurane ordioxane, liquid aromatic hydrocarbons, such as benzene or toluene,alcohols, such as methanol, ethanol or 1- or 2-propanol, nitriles, suchas acetonitrile, halogenated hydrocarbons, such as methylene chloride orchloroform, acid amides, such as dimethylformamide or dimethylacetamide, bases, such as heterocyclic nitrogen bases, for examplepyridine or N-methylpyrrolidin-2-one, carboxylic acid anhydrides, suchas lower alkanoic acid anhydrides, for example acetic anhydride, cyclic,linear or branched hydrocarbons, such as cyclohexane, hexane orisopentane, or mixtures of those solvents, for example aqueoussolutions, unless otherwise indicated in the description of theprocesses. Such solvent mixtures may also be used in working up, forexample by chromatography or partitioning.

The compounds, including their salts, may also be obtained in the formof hydrates, or their crystals may, for example, include the solventused for crystallization. Different crystalline forms may be present.

The invention relates also to those forms of the process in which acompound obtainable as an intermediate at any stage of the process isused as starting material and the remaining process steps are carriedout, or in which a starting material is formed under the reactionconditions or is used in the form of a derivative, for example in aprotected form or in the form of a salt, or a compound obtainable by theprocess according to the invention is produced under the processconditions and processed further in situ.

EXEMPLIFICATION OF THE INVENTION

The invention is further illustrated by the following examples, whichshould not be construed to limit the scope of the invention.Demonstration of efficacy in these assays is predictive of efficacy insubjects.

General Synthesis Methods

All starting materials, building blocks, reagents, acids, bases,dehydrating agents, solvents, and catalysts utilized to synthesis thecompounds of the present invention are either commercially available orcan be produced by organic synthesis methods known to one of ordinaryskill in the art (Houben-Weyl 4th Ed. 1952, Methods of OrganicSynthesis, Thieme, Volume 21). Further, the compounds of the presentinvention can be produced by organic synthesis methods known to one ofordinary skill in the art as shown in the following examples.

LIST OF ABBREVIATIONS

-   Ac acetyl-   ACN Acetonitrile-   AcOEt/EtOAc Ethyl acetate-   AcOH acetic acid-   aq aqueous-   Ar aryl-   Bn benzyl-   Bu butyl (nBu=n-butyl, tBu=tert-butyl)-   CDI Carbonyldiimidazole-   CH₃ CN Acetonitrile-   DBU 1,8-Diazabicyclo[5.4.0]-undec-7-ene-   DCE 1,2-Dichloroethane-   DCM Dichloromethane-   DIPEA N-Ethyldiisopropylamine-   DMAP Dimethylaminopyridine-   DMF N,N′-Dimethylformamide-   DMSO Dimethylsulfoxide-   EI Electrospray ionisation-   Et₂O Diethylether-   Et₃N Triethylamine-   Ether Diethylether-   EtOH Ethanol-   FC Flash Chromatography-   h hour(s)-   HATU O-(7-Azabenzotriazole-1-yl)-N,N,N′N′-tetramethyluronium    hexafluorophosphate-   HBTU O-(Benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium    hexafluorophosphate-   HCl Hydrochloric acid-   HOBt 1-Hydroxybenzotriazole-   HPLC High Performance Liquid Chromatography-   H₂O Water-   L liter(s)-   LC-MS Liquid Chromatography Mass Spectrometry-   Me methyl-   MeI Iodomethane-   MeOH Methanol-   mg milligram-   min minute(s)-   mL milliliter-   MS Mass Spectrometry-   Pd/C palladium on charcoal-   PG protecting group-   Ph phenyl-   Prep Preparative-   Rf ratio of fronts-   RP reverse phase-   Rt Retention time-   rt Room temperature-   SiO₂ Silica gel-   TBAF Tetrabutylammonium fluoride-   TEA Triethylamine-   TFA Trifluoroacetic acid-   THF Tetrahydrofurane-   TLC Thin Layer Chromatography

HPLC Methods: Method A: HPLC

Instrument: Agilent systemColumn: Zorbax eclipse XDB-C18, 1.8 microm., 2.1×50 mm, flow 1 mL/min

Solvent: CH3CN (0.1% CF3CO2H), H2O (0.1% CF3CO2H) Gradient: 0-0.8 min:10-95% CH3CN, 0.8-1.2 min: 95% CH3CN, 1.2-1.6 min 95% to 10% CH3CNMethod A2: HPLC

Instrument: Agilent systemColumn: MN Nucleosil C18HD CC70, 4 microm, 2.1×50 mm, flow 1 mL/min

Solvent: CH3CN (0.1% CF3CO2H), H2O (0.1% CF3CO2H) Gradient: 0-6 min:20-100% CH3CN, 6-7.5 min: 100% CH3CN, 7.5-8.0 min 100-20% CH3CN MethodA3: HPLC

Instrument: Agilent systemColumn: Agilent Eclipse, 1.8 microm., 4.6×50 mm, flow 1 mL/min

Solvent: CH3CN (0.1% CF3CO2H), H2O (0.1% CF3CO2H) Gradient: 0-6 min:20-100% CH3CN, 6-7.5 min: 100% CH3CN, 7.5-8.0 min 100-20% CH3CN MethodA4: LCMS

Instrument: Agilent systemColumn: Inertsil C8-3; 3.0×30 mm; 3 μm particle size, flow 2 mL/minSolvent: CH3CN, H2O (5 mM ammonium formate)Gradient: 0-1.7 min: 5-95% CH3CN, hold for 0.3 min, 2-2.1 min 95-5%CH3CN

Method A5: LCMS

Instrument: Agilent systemColumn: Inertsil ODS-3; 3.0×30 mm; 3 μm particle size, flow 2 mL/minSolvent: CH3CN, H2O (5 mM ammonium formate)Gradient: 0-1.7 min: 20-95% CH3CN, hold for 0.3 min, 2-2.1 min 95-20%CH3CN

Method A6: LCMS

Instrument: Agilent systemColumn: Waters Atlantis dC18; 4.6×150 mm; 5 μm particle size, flow 1.41mL/min

Solvent: CH3CN (0.07% TFA), H2O (0.1% TFA)

Gradient: 0-19 min: 5-95% CH3CN, hold for 0.8 min

Method B: HPLC

Instrument: Agilent systemColumn: Waters Symmetry C18, 3.5 microm., 2.1×50 mm, flow 0.6 mL/min

Solvent: CH3CN (0.1% CF3CO2H), H2O (0.1% CF3CO2H) Gradient: 0-3.5 min:20-95% CH3CN, 3.5-5 min: 95% CH3CN, 5.5-5.55 min 95% to 20% CH3CN MethodC: HPLC

Instrument: Agilent systemColumn: MN Nucleosil C18HD CC70, 4 microm., flow 0.6 mL/min

Solvent: CH3CN (0.1% CF3CO2H), H2O (0.1% CF3CO2H) Gradient: 0-3.5 min:20-95% CH3CN, 3.5-5 min: 95% CH3CN, 5.5-5.55 min 95% to 20% CH3CN,5.55-6 min 20% CH3CN Method D: HPLC

Instrument: Agilent system

Column: Waters SunFire, 2.5 microm., 3×30 mm, flow 1.4 mL/min

Solvent: CH3CN (0.1% CF3CO2H), H2O (0.1% CF3CO2H) Gradient: 0-2.5 min:10-98% CH3CN, 2.5-3.2 min: 98% CH3CN, 3.2-3.21 min 98% to 10% CH3CN,3.21-3.25 min 10% CH3CN Method E: LCMS

Instrument: Agilent systemColumn: Waters SunFire, 2.5 microm., 3×30 mm, flow 1.4 mL/min

Solvent: CH3CN (0.1% HCO2H), H2O (0.1% HCO2H) Gradient: 0-2.5 min:10-98% CH3CN, 2.5-3.2 min: 98% CH3CN, 3.2-3.21 min 98% to 10% CH3CN,3.21-3.25 min 10% CH3CN Method F: LCMS

Instrument: Agilent systemColumn: Waters SunFire, 2.1×50 mm, flow 0.6 mL/min

Solvent: CH3CN (0.1% HCO2H), H2O (0.1% HCO2H) Gradient: 0-2.5 min:10-98% CH3CN, 2.5-3.2 min: 98% CH3CN, 3.2-3.21 min 98% to 10% CH3CN,3.21-3.25 min 10% CH3CN Method G: LCMS

Instrument: Agilent systemColumn: Halo C18, 2.7 microm., 2.1×30 mm, flow 1.1 mL/min

Solvent: CH3CN (0.1% HCO2H), H2O (0.1% HCO2H) Gradient: 0-2 min: 5-95%CH3CN, 2-2.6 min: 95% CH3CN, 2.6-2.65 min 95% to 5% CH3CN, 2.65-3 min 5%CH3CN Method H: LCMS

Instrument: Agilent systemColumn: YMC ODS, 2.5 microm., 2.1×50 mm, flow 0.6 mL/min

Solvent: CH3CN (0.1% HCO2H), H2O (0.1% HCO2H) Gradient: 0-3.5 min:20-95% CH3CN, 3.5-5.5 min: 95% CH3CN, 5.5-5.55 min 95% to 20% CH3CN,5.55-6 min 20% CH3CN Method I: LCMS

Instrument: Agilent systemColumn: Waters Atlantis, 2.1×30 mm, flow 0.6 mL/min

Solvent: CH3CN (0.1% HCO2H), H2O (0.1% HCO2H) Gradient: 0-2.5 min:20-95% CH3CN, 2.5-4.5 min: 95% CH3CN, 4.5-4.55 min 95% to 20% CH3CN,4.55-5 min 20% CH3CN Method I2: LCMS

Instrument: Agilent systemColumn: Waters Atlantis, 2.1×30 mm, flow 0.6 mL/min

Solvent: CH3CN (0.1% HCO2H), H2O (0.1% HCO2H) Gradient: 0-2.5 min: 5-95%CH3CN, 2.5-4.5 min: 95% CH3CN, 4.5-4.55 min 95% to 5% CH3CN, 4.55-5 min5% CH3CN Method I3: LCMS

Instrument: Agilent systemColumn: Waters Atlantis, 3.0 microm., 2.1×30 mm, flow 0.6 mL/min

Solvent: CH3CN (0.1% HCO2H), H2O (0.1% HCO2H) Gradient: 0-3.5 min:20-95% CH3CN, 3.5-4.5 min: 95% CH3CN, 4.5-4.55 min 95% to 20% CH3CN,4.55-5 min 20% CH3CN Method J: MS

Instrument: Agilent systemMethod: Flow injectionDetection: API-ES, positive/negative

Method K: Preparative HPLC

Instrument: Gilson systemcolumn: waters C18 ODB, 5 microm, 50×19 mmsolvent: CH3CN (0.1% HCO2H); H2O (0.1% HCO2H)

Method L: Preparative HPLC

Instrument: Gilson

Column: Sun-Fire prep C18 OBD 5 microm, Column 19×50 mm (flow 20 mL/min)or column 30×100 mm (flow 40 mL/min)

Solvent: CH3CN (0.1% CF3CO2H) and H2O (0.1% CF3CO2H) Gradient: 0-20 min:5-100% CH3CN Method M: HPLC-MS Instrument: Waters

Column: Waters Atlantis, 2.1×30 mm, flow 0.6 mL/min

Solvent: CH3CN (0.1% HCO2H), H2O (0.1% HCO2H) Gradient: 0-2.5 min:20-95% CH3CN, 2.5-4.5 min: 95% CH3CN, 4.5-4.55 min 95% to 20% CH3CN,4.55-5 min 20% CH3CN Preparation of Intermediate I

Step 1a

A suspension ofN-(tert-butoxycarbonyl)-N-[4-(dimethylazaniumylidene)-1,4-dihydropyridin-1-ylsulfonyl]azanide(3 g; 9.955 mmol) prepared according to the procedure from Winum et al(Organic Letters 2001, 3, 2241) in DCM (24 mL) was treated withpyrrolidine (0.864 mL; 10.453 mmol) and stirred at rt for 24 h. Thereaction mixture was chromatographed by FC on silica gel (eluent: CH₂Cl₂/EtOAc 100:1) to give[N-(tert-butoxycarbonyl)]-pyrrolidine-1-sulfonic acid amide. TLC: Rf(DCM/EtOAc 100:1)=0.40. A solution of[N-(tert-butoxycarbonyl)]-pyrrolidine-1-sulfonic acid amide (57.09 g;223 mmol) in DCM (450 mL) was treated with TFA (120 mL; 1.56 mol) andstirred at rt for 7 h. The reaction mixture was concentrated in vacuoand the residual oil was triturated with diisopropylether. The resultingpowder was washed with diisopropylether and dried under high vacuum toprovide Compound 1a. TLC: Rf (DCM/EtOAc 50:1)=0.10.

Step 1b

A solution of(1R,2S)-1-tert-butoxycarbonylamino-2-vinyl-cyclopropanecarboxylic acidprepared according to the procedure described in WO2000/09558 (8.24 g;36.3 mmol) in THF (160 mL) was treated with CDI (9.09 g; 54.4 mmol) andheated to reflux for 1 h. The resulting reaction mixture was cooled tort and treated with Compound 1a (7.62 g; 50.8 mmol) followed by DBU(8.28 g; 54.4 mmol). After 16 h at rt the reaction mixture wasconcentrated, the residue was taken up in DCM and washed with asaturated aq solution of KHSO₄ (3×). The aq phases were extracted withDCM, the organics were combined, dried over Na₂SO₄ and concentrated invacuo. The residue was chromatographed on silica gel (eluent:hexane/EtOAc 4:1) to give Compound 1b. LCMS (method F) Rt=3.21 min; MS(method J): M/z=358 [M−1]

Step 1c

Compound 1b (7.84 g; 21.81 mmol) was treated with 4N HCl in dioxane (84mL) at rt. After 1.5 h the reaction mixture was concentrated under highvacuum to give Compound 1c as its hydrochloride salt. LCMS (method E)Rt=1.10 min; MS (method J): M/z=260 [M+1]

Step 1d

(5R,8S)-10,10-dimethyl-7-aza-dispiro[3.0.4.1]decane-7,8-dicarboxylicacid 7-tert-butyl ester is prepared by the procedure provided at page113, line 12 to page 114, line 7 of copending international patentapplication PCT/EP08/063,460, which passage is expressly incorporatedherein by reference. A solution of Compound 1c hydrochloride (1.363 g;4.01 mmol) and(5R,8S)-10,10-dimethyl-7-aza-dispiro[3.0.4.1]decane-7,8-dicarboxylicacid 7-tert-butyl ester (1.24 g; 4.01 mmol) in DMF (20 mL) was treatedwith DIPEA (2.745 mL; 16.03 mmol), cooled to 0° C. and treated with HBTU(1.9 g; 5.01 mmol). The reaction mixture was stirred at 0° C. for 1 hand at rt for 19 h, partitioned between water and EtOAc: The organicswere washed sequentially with saturated aq KHSO₄, NaCO₃ and water, driedover Na₂SO₄ and concentrated in vacuo. The residue was chromatographedon silica gel (eluent: DCM/MeOH 50:1) to give Compound 1d. TLC: Rf(DCM/MeOH 98:2)=0.28; MS (method J): M/z=549 [M−1]

Step 1e

Compound 1e hydrochloride was obtained from Compound 1d (0.296 g; 0.537mmol) according to the method described at step 1c. TLC: Rf (DCM/MeOH9:1)=0.48; MS (method J): M/z=451 [M+1]

Step 1f

A solution of Compound 1e (0.287 g; 0.536 mmol) and BOC-L-tert-leucine(0.248 g; 1.072 mmol) in DCM (15 mL) was cooled to 0° C. and treatedwith DIPEA (0.46 mL; 2.68 mmol) and HATU (0.611 g; 1.608 mmol). Thereaction mixture was stirred at rt for 20 h, concentrated in vacuo andthe residue was purified by preparative HPLC (method K). After workup(Workup 2=fractions were treated with NaHCO₃ and concentrated; residuepartitioned between water and EtOAc, extracted with EtOAc; organicscombined, dried over Na₂SO₄ and concentrated) Compound 1f was obtained.TLC: Rf (DCM/MeOH 96:4)=0.70; MS (method J): M/z=662 [M−1]

Step 1g

Compound 1g hydrochloride was obtained from Compound 1f (0.204 g; 0.307mmol) according to the method described at step 1c. TLC: Rf (DCM/MeOH9:1)=0.39; MS (method J): M/z=564 [M+1]

Step 1h

A solution of Compound 1g (1.845 g; 3.07 mmol) andBOC-L-cyclohexylglycine (1.582 g; 6.15 mmol) in DCM (65 mL) was cooledto 0° C. and treated with DIPEA (2.68 mL; 15.37 mmol) followed by HATU(3.51 g; 9.22 mmol). After 16 h at rt the reaction mixture waspartitioned between DCM and 1N HCl, the organics were extracted withsaturated aq NaHCO₃, dried over Na₂SO₄ and concentrated. Purification bypreparative HPLC (method K) followed by workup (Workup 2) affordedCompound 1h. LC-MS (method E): Rt=3.18 min; M/z=826 [M+Na]

Step 1i

Intermediate I hydrochloride was obtained from Compound 1h (1.64 g;2.042 mmol) according to the method described at step 1c. LC-MS (methodE): Rt=1.95 min; M/z=703 [M+1]

Preparation of Intermediate II

Step 2a

(5R,8S)-10,10-Dimethyl-7-aza-dispiro[3.0.4.1]decane-7,8-dicarboxylicacid 7-tert-butyl ester

(32.84 g; 106 mmol) in DMF (1 L) was treated with K₂CO₃ (22.00 g; 159mmol) followed by methyliodide (9.93 mL; 159 mmol). The reaction mixturewas stirred at rt for 18 h, concentrated in vacuo. The resulting residuewas partitioned between water and EtOAc and extracted with EtOAc. Theorganics were combined, washed with brine, dried over Na₂SO₄ andconcentrated. The residue was chromatographed on silica gel (eluentDCM/Ethylether 120:1) to give Compound 2a. TLC: Rf (DCM/Ethylether120:1)=0.22; MS (method J): M/z=346 [M+Na]

Step 2b

Compound 2b hydrochloride was obtained from Compound 2a (6.3 g; 19.48mmol) according to the method described at step 1c. MS (method J):M/z=224 [M+1]

Step 2c

Compound 2c was obtained from Compound 2b hydrochloride (7.33 g; 27.93mmol) according to the method described at step 1f followed bychromatography on silica gel (eluent cyclohexane/EtOAc 1:1). TLC: Rf(hexane/EtOAc 4:1)=0.37; MS (method J): M/z=437 [M+1]

Step 2d

Compound 2d hydrochloride was obtained from Compound 2c (10.55 g; 24.16mmol) according to the method described at step 1c. TLC: Rf (DCM/MeOH95:5)=0.39; MS (method J): M/z=337 [M+1]

Step 2e

Compound 2e was obtained from Compound 2d (0.2 g; 0.456 mmol) accordingto the method described at step 1h. LC-MS (method G): Rt=2.21 min;M/z=598 [M+Na]

Step 2f

A mixture of Compound 2e (1.136 g; 1.973 mmol) and LiOH.H₂O (0.09 g;2.17 mmol) in THF/MeOH/water (6 mL; 2:1:1) was stirred at rt 16 h. Thereaction mixture was partitioned between water and EtOAc. The aq phasewas acidified with 1N HCl and extracted with EtOAC. Organics werecombined, dried over Na₂SO₄ and concentrated to a residue that waschromatographed on silica gel (DCM/MeOH 100% to 9:1) to afford Compound2f. LC-MS (method G): Rt=1.99 min; M/z=562 [M+1]

Step 2g

A solution of Compound 2f (0.050 g; 0.089 mmol) andpyrrolidine-1-sulfonic acid((1R,2R)-1-amino-2-ethyl-cyclopropanecarbonyl)-amide (0.030 g; 0.093mmol) in DCM (2 mL) was cooled to 0° C. and treated with DIPEA (0.078mL; 0.445 mmol) and HATU (0.102 g; 0.267 mmol). The reaction mixture wasstirred at rt for 2 h, partitioned between DCM and 1N HCl. The organicswere washed with a saturated aq NaHCO₃ solution, dried over Na₂SO₄ andconcentrated in vacuo to a residue that was purified by preparativeHPLC. After workup (Workup 2) Compound 2g was obtained. LC-MS (methodG): Rt=2.25 min; M/z=828 [M+Na]

Step 2h

Intermediate II hydrochloride was obtained from Compound 2g (0.02 g;0.025 mmol) according to the method described at step 1c. LC-MS (methodG): Rt=1.59 min; M/z=706 [M+1]

Preparation of Intermediate III pyrrolidine-1-sulfonic acid((1R,2R)-1-amino-2-ethyl-cyclopropanecarbonyl)-amide

Step 3a

A solution of(1R,2S)-1-tert-butoxycarbonylamino-2-vinyl-cyclopropanecarboxylic acidmethyl ester prepared according to the procedure described in WO20009558(60.16 g; 249 mmol) in 2 L EtOH was hydrogenated at RT under H₂,catalyzed by Rh—Al₂O₃ (5 g). Under completion, the catalyst was filteredoff and the solution concentrated under high vacuum to afford Compound3a. MS (method J): M/z=266 [M+Na]

A mixture of Compound 3a (10 g; 41.1 mmol) and LiOH.H₂O (5.17 g; 123mmol) in THF/MeOH/water (440 mL; 2:1:1) was stirred at rt for 20 h. Thereaction mixture was concentrated. The resulting aq phase was washedwith EtOAc, cooled to 5° C., acidified with 6N HCl and extracted withEtOAC. Organics were combined, dried over Na₂SO₄ and concentrated to aresidue that was crystallized from cyclohexane to afford Compound 3b.LC-MS (method G): Rt=1.40 min; M/z=252 [M+Na]

Step 3c

Compound 3c was obtained from Compound 3b (5 g; 21.81 mmol) according tothe method described at step 1b. LC-MS (method D): Rt=1.91 min; M/z=360[M-1]

Step 3d

Pyrrolidine-1-sulfonic acid((1R,2R)-1-amino-2-ethyl-cyclopropanecarbonyl)-amide hydrochloride wasobtained from Compound 3c (4.602 g; 12.73 mmol) according to the methoddescribed at step 1c. LC-MS (method E): Rt=1.06 min; M/z=262 [M+1]

Example 1 Compound 13

A suspension of (S)-1-isopropyl-piperidine-2-carboxylic acid (1.39 g;8.11 mmol) in DMF (150 mL) was treated with HATU (3.86 g; 10.14 mmol)and DIPEA (3.54 mL; 20.29 mmol) and stirred at RT. The resultingsolution was treated with Intermediate I hydrochloride (5 g; 6.76 mmol)and stirred at RT under Argon for 1 h. The reaction mixture was taken upin EtOAc, washed with water. The aqueous phase was extracted with EtOAc.The organics were combined, washed with saturated aq NaHCO₃, dried overNa₂SO₄ and concentrated to a brown oil. Purification by FC on silica gel(eluent: cyclohexane to cyclohexane/aceton 3:2) afforded Compound 1as afoam. TLC: Rf (cyclohexane/aceton 3:2)=0.23; LC-MS (method E): M/z=856[M+1]; HPLC (method D): Rt=2.13 min; 1H-NMR (500 MHz, DMSO-d6): δ(ppm)=10.2 (s, 1H), 9.6 (bs, 1H), 8.9 (d, 1H), 8.8 (s, 1H), 8.0 (d, 1H),5.5 (dt, 1H), 5.2 (d, 1H), 5.1 (d, 1H), 4.55 (d, 1H), 4.35 (t, 1H), 4.15(t, 1H), 4.05 (t, 1H), 3.4-3.65 (m, 5H), 3.3 (m, 4H), 3.1 (m, 2H), 2.85(bs, 1H), 2.5 (t, 1H), 2.15 (m, 1H), 0.9-2.0 (m, 42H), 0.85 (s, 3H), 0.8(s, 3H).

Example 2 Compound 34

Compound 2 hydrochloride was obtained from Intermediate II (0.28 g;0.378 mmol) according to the method described for the preparation ofCompound 1. HPLC (method B): Rt=3.70 min; MS (method J) M/z=858 [M+1]

1H-NMR (400 MHz, methanol-d4): δ (ppm)=8.4 (d, 1H), 4.75 (d, 1H), 4.3(d, 1H), 4.2 (t, 1H), 3.95 (bs, 1H), 3.4-3.7 (m, 9H), 3.0 (m, 1H), 2.15(m, 1H), 1.05-2.1 (m, 43H), 1.05 (s, 9H), 0.9 (s, 3H), 0.95 (s, 3H).

The following compounds were prepared in an analogous manner:

Example 3 Compound 15

1H-NMR (500 MHz, DMSO-d6): δ (ppm)=10.1 (s, 1H), 9.15 (bs, 1H), 8.75 (s,1H), 8.65 (d, 1H), 8.0 (d, 1H), 5.5 (m, 1H), 5.2 (d, 1H), 5.1 (d, 1H),4.55 (d, 1H), 4.4 (t, 1H), 4.25 (m, 1H), 4.1 (t, 1H), 3.4-3.6 (m, 4H),3.2 (m, 1H), 2.3 (m, 1H), 2.1 (m, 1H), 1.2 (d, 3H), 1.15 (d, 3H),0.9-2.0 (m, 32H), 0.95 (s, 9H), 0.85 (s, 3H), 0.8 (s, 3H).

Example 4 Compound 37

1H-NMR (400 MHz, methanol-d4): δ (ppm)=8.4 (d, 1H), 5.75 (dt, 1H), 5.2(d, 1H), 5.1 (d, 1H), 4.7 (d, 1H), 4.3 (d, 1H), 4.2 (t, 1H), 3.8 (bs,1H), 3.35-3.7 (m, 7H), 2.9-3.3 (m, 3H), 2.2 (m, 1H), 1.1 (m, 35H), 1.05(s, 9H), 0.9 (s, 3H), 0.95 (s, 3H).

Example 5 Compound 63

1H-NMR (500 MHz, DMSO-d6): δ (ppm)=10.2 (s, 1H), 8.8 (s, 1H), 8.05 (d,1H), 7.75 (d, 1H), 5.55 (m, 1H), 5.2 (d, 1H), 5.1 (d, 1H), 4.5 (d, 1H),4.4 (t, 1H), 4.1 (t, 1H), 3.5 (m, 2H), 3.2 (m, 4H), 3.1 (bs, 1H), 2.8(m, 1H), 2.4 (m, 2H), 2.2 (m, 1H), 2.1 (m, 2H), 1.5-1.95 (m, 17H), 1.25(t, 1H), 0.9-1.15 (m, 24H), 0.85 (s, 3H), 0.8 (s, 3H).

Example 6 Compound 65

1H-NMR (500 MHz, DMSO-d6): δ (ppm)=10.15 (s, 1H), 9.5 (t, 1H), 8.8 (m,2H), 8.0 (d, 1H), 5.55 (dt, 1H), 5.2 (d, 1H), 5.1 (d, 1H), 4.55 (d, 1H),4.35 (t, 1H), 4.1 (t, 1H), 4.0 (m, 1H), 3.6 (d, 1H), 3.5 (d, 1H), 3.3(m, 5H), 2.9 (bs, 1H), 2.1 (m, 1H), 1.0-2.0 (m, 34H), 1.1 (t, 6H), 1.0(s, 9H), 0.9 (s, 3H), 0.85 (s, 3H).

Example 7 Compound 93

1H-NMR (500 MHz, DMSO-d6): δ (ppm)=10.2 (s, 1H), 9.5 (bs, 1H), 8.75 (s,1H), 8.65 (d, 1H), 8.0 (d, 1H), 5.55 (m, 1H), 5.2 (d, 1H), 5.1 (d, 1H),4.5 (d, 1H), 4.4 (t, 1H), 4.1 (t, 1H), 3.75 (t, 1H), 3.5 (m, 2H), 3.15(m, 2H), 3.0 (m, 1H), 2.75 (m, 3H), 2.65 (m, 3H), 2.1 (m, 1H), 1.05-2.0(m, 28H), 1.05 (t, 3H), 0.9 (s, 9H), 0.85 (s, 3H), 0.8 (s, 3H).

Example 8 Compound 95

1H-NMR (500 MHz, DMSO-d6): δ (ppm)=10.2 (s, 1H), 9.56 (bs, 1H), 8.7 (m,2H), 8.05 (d, 1H), 5.55 (m, 1H), 5.25 (d, 1H), 5.1 (d, 1H), 4.55 (d,1H), 4.4 (t, 1H), 4.15 (t, 1H), 3.5 (m, 2H), 3.0-3.5 (m, 8H), 0.75-2.5(m, 28H), 0.95 (s, 9H), 0.85 (s, 3H), 0.8 (s, 3H).

Example 9 Compound 108

1H-NMR (500 MHz, DMSO-d6): δ (ppm)=10.1 (s, 1H), 9.5 (bs, 1H), 8.8 (s,1H), 8.75 (d, 1H), 8.05 (d, 1H), 6.0 (dt, 1H), 5.25 (d, 1H), 5.1 (d,1H), 4.55 (m, 1H), 4.4 (m, 1H), 4.1 (t, 1H), 4.0 (m, 2H), 3.55 (m, 3H),2.9 (m, 1H), 2.7 (s, 3H), 2.1 (m, 1H), 1.0-2.0 (m, 34H), 1.05 (t, 6H),1.0 (s, 9H), 0.9 (s, 3H), 0.85 (s, 3H).

Example 10 Compound 120

1H-NMR (500 MHz, DMSO-d6): δ (ppm)=10.1 (s, 1H), 9.4 (bs, 1H), 8.8 (s,1H), 8.75 (d, 1H), 8.05 (d, 1H), 5.6 (dt, 1H), 5.2 (d, 1H), 5.05 (d,1H), 4.55 (d, 1H), 4.35 (t, 1H), 4.1 (t, 1H), 3.95 (t, 1H), 3.5 (m, 2H),3.35-3.4 (m, 4H), 3.2 (m, 2H), 2.85 (bs, 1H), 2.1 (m, 1H), 0.9-2.0 (m,50H), 0.85 (s, 3H), 0.8 (s, 3H).

Example 11 Compound 142

1H-NMR (500 MHz, DMSO-d6): δ (ppm)=10.15 (s, 1H), 9.5 (bs, 1H), 8.75 (d,1H), 8.65 (s, 1H), 8.05 (d, 1H), 4.55 (d, 1H), 4.4 (t, 1H), 4.1 (t, 1H),4.0 (t, 1H), 3.55 (m, 2H), 3.45 (m, 1H), 3.15 (m, 1H), 3.05 (m, 1H),2.85 (m, 1H), 2.77 (s, 3H), 0.75-2.0 (m, 45H), 0.95 (s, 9H), 0.85 (s,3H), 0.8 (s, 3H).

Example 12 Compound 99

mixture of 100 mg (0.14 mmol)(5R,8S)-7-[(2S)-2-{[(2S)-2-amino-2-cyclohexylacetyl]amino}-3,3-dimethylbutanoyl]-N-{(1R,2R)-2-ethyl-1-[(pyrrolidin-1-ylsulfonyl)carbamoyl]cyclopropyl}-10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8-carboxamide(hydrochloride salt), 20 mg (0.14 mmol)(S)-1-ethyl-pyrrolidine-2-carboxylic acid (lithium salt), 77 mg (0.20mmol) HATU and 0.1 mL (0.61 mmol) DIPEA in 4 mL DMF was stirred at RTfor 1 h. The reaction mixture was diluted with DCM and washed with 10%aq. KHSO₄ solution. The aq. layer was extracted with DCM (3×) and thecombined organic layers were washed with sat. aq. NaHCO₃ solution, driedover Na₂SO₄ and concentrated in vacuo. The crude product was purified byprep. HPLC to yield the title compound. LC-MS (method E): Rt=1.862 min;M/z=830.5 [M+H]; HPLC (method D): Rt=2.093 min. 1H-NMR (500 MHz,DMSO-d6): d=0.83 (s, 3H), 0.86 (s, 3H), 0.88-0.91 (m, 5H), 0.93 (s, 9H),1.28-1.44 (m, 6H), 1.52-1.80 (m, 22H), 1.83-1.90 (m, 5H), 2.04-2.07 (m,1H), 2.23-2.26 (m, 1H), 2.40-2.47 (m, 2H), 2.84-2.85 (m, 1H), 3.11-3.13(m, 1H), 3.31-3.34 (m, 4 H), 3.49-3.54 (m, 2H), 4.11 (dd, 1H), 4.41 (dd,1H), 4.53 (d, 1H), 7.78 (d, 1H), 8.04 (d, 1H), 8.55 (bs, 1H).

Example 13 Compound 100

A mixture of 100 mg (0.14 mmol)(5R,8S)-7-[(2S)-2-{[(2S)-2-amino-2-cyclohexylacetyl]amino}-3,3-dimethylbutanoyl]-N-[(1R,2R)-1-{[(diethylamino)sulfonyl]carbamoyl}-2-ethylcyclopropyl]-10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8-carboxamide(hydrochloride salt) (prepared in analogy as described for intermediateI starting with diethyl amine instead of pyrrolidine), 29 mg (0.20 mmol)(S)-1-ethyl-pyrrolidine-2-carboxylic acid (lithium salt), 102 mg (0.27mmol) HATU and 0.1 mL (0.60 mmol) DIPEA in 3 mL DCM was stirred at RTovernight. The reaction mixture was concentrated in vacuo and the crudewas purified by prep. HPLC to yield the title compound. LC-MS (methodE): Rt=2.636 min; M/z=830.5 [M−H]; HPLC (method B): Rt=3.813 min. 1H-NMR(500 MHz, CDCl3): d=0.91 (s, 3H), 0.94 (s, 3H), 1.00 (t, 3H), 1.02 (s, 9H), 1.06-1.13 (m, 7H), 1.22 (t, 6H), 1.71-2.00 (m, 15H), 2.12-2.23 (m,2H), 2.32-2.41 (m, 1H), 2.51-2.58 (m, 1H), 2.61-2.69 (m, 1H), 3.10-3.13(m, 1H), 3.21-3.24 (m, 1H), 3.35-3.46 (m, 4 H), 3.52-3.62 (m, 2H),4.28-4.35 (m, 2H), 4.76 (d, 1H), 7.03 (bs, 1H), 8.08 (d, 1H), 9.90 (bs,1 H).

Example 14 Compound 174

Prepared in analogy to example 100

1H NMR (400 MHz, CHLOROFORM-d) δ ppm 0.82 (d, 9H) 0.88-1.03 (m, 7H)1.04-1.22 (m, 3H) 1.09 (t, 12H) 1.26 (br. s., 2H) 1.65 (br. s., 8H) 1.83(br. s., 8H) 1.97 (br. s., 2H) 2.10 (br. s., 2H) 2.37 (br. s., 1H) 2.55(br. s., 1H) 2.72 (br. s., 1H) 3.19-3.36 (m, 1H) 3.29 (ddd, 3H) 3.39(br. s., 1H) 3.45 (br. s., 2H) 3.58 (s, 1H) 3.94 (br. s., 1H) 4.20 (br.s., 1H) 4.58 (br. s., 1 H) 5.05 (s, 1H) 5.19 (s, 1H) 5.61 (s, 1H) 6.62(br. s., 1H) 6.94 (d, 1H) 9.36 (br. s., 1H) 9.74 (br. s., 1H) 11.97 (br.s., 1H)

Example 15 Compound 203

Step a

2 was prepared by a modification of the procedure published in theliterature (J. Org. Chem., 2005, 70, 5869). 1 (1.004 g, 4.40 mmol) wasdissolved in TBME (25 ml) and hydrogenated (1 atm hydrogen gas) over 20%Pd(OH)₂/C (150 mgs) for 3 hours. The suspension was then filtered oncelite and the crude concentrated under reduced pressure. The crude iscrystallized from water-ethanol. The crude is taken in 100 ml water andheated to 70° C. and ethanol is added drop wise until the solutionbecomes clear. The solution is left overnight to cool and the solids arefiltered to get the pure product 2 (494 mgs, 2.155 mmol, 49% yield). Thepure product is dried under vacuum.

Step b

To 2 (100 mg, 0.436 mmol) in DMF (2 ml), CDI (150 mgs, 0.925 mmol) isadded and stirred and heated to 100° C. for 1 hour. To the stirredsolution 3 (100 mgs, 0.657 mmol) and DBU (0.5 ml, 3.32 mmol) are addedand stirred to room temperature over night. The crude is diluted withethyl acetate (25 ml) and washed successively with 1 M Sulfuric acid(3×100 ml) and saturated brine (. {tilde over (x)}. iml). The ethylacetate layer containing the product is then concentrated under reducedpressure and purified on a silica column using 0-50% ethyl acetate inheptane as an eluent to get the pure product, 4 (64 mgs, 0.176 mmol,40%).

1H NMR (400 MHz, CHLOROFORM-d) 1.00 (t, J=7.20 Hz, 3H) 1.05-1.13 (m, 1H)1.22 (t, J=7.20 Hz, 6H) 1.36-1.43 (m, 1H) 1.48 (s, 9H) 1.56 (br. s., 4H)3.42 (dd, 4H) 4.67-5.59 (m, 1H)

Step c

4 (64 mgs, 0.176 mmol) is dissolved in DCM (1 ml) and 4M HCl in dioxane(1 ml) was added and stirred at 32° C. for 1 hour until the deprotectionis complete to yield the crude 5. The crude is concentrated underreduced pressure and is taken to the next step without furtherpurification.

Step d

To(5R,8S)-7-((S)-2-{(S)-2-Cyclohexyl-2-[((S)-1-isopropyl-piperidine-2-carbonyl)-amino]-acetylamino}-3,3-dimethyl-butyryl)-10,10-dimethyl-7-aza-dispiro[3.0.4.1]decane-8-carboxylicacid (see example 150 step c) (90 mg, 0.146 mmol) and 5 (55 mg, 0.210mmol) in DMF (1 ml), DIPEA (0.5 ml, 2.86 mmol) is added followed by HATU(80 mg, 0.210 mol) and the reaction is stirred to completion. The crudeis diluted with ethyl acetate and washed with saturated brine to removeDMF. The crude ethyl acetate layer is concentrated under reducedpressure and taken for purification. A HPLC purification using ammonia(0.1%) in Acetonitrile-water yields the product (4 mg, 0.0046 mmol, 3%yield)

1H NMR (400 MHz, CHLOROFORM-d) δ ppm 0.83 (d, 8H) 0.98 (br. s., 1H) 1.00(s, 9H) 1.09-1.26 (m, 11H) 1.54 (d, 10H) 1.63 (br. s., 2H) 1.68 (br. s.,4H) 1.87 (d, 8H) 2.09 (br. s., 1H) 2.26 (s, 1H) 2.40 (br. s., 1H) 2.61(br. s., 1H) 3.22 (d, 1H) 3.24 (s, 1H) 3.33 (s, 1H) 3.31 (d, 2 H) 3.44(s, 2H) 3.53 (s, 2H) 3.95 (br. s., 1H) 4.23 (s, 2H) 4.58 (s, 1H) 6.64(br. s., 1H) 6.93 (s, 1H) 9.42 (br. s., 1H) 9.69 (s, 1H) 12.00 (br. s.,1H)

Example 16 Compound 145

A solution of (S)-1-D₇-isopropyl-piperidine-2-carboxylic acid (0.039 g;0.108 mmol), DIPEA (0.047 mL; 0.27 mmol) and HATU (0.041 g; 0.108 mmol)in DMF (2 mL) was stirred for 15 min at ambient temperature. Afteraddition of(5R,8S)-7-[(S)-2-((S)-2-Amino-2-cyclohexyl-acetylamino)-3,3-dimethyl-butyryl]-10,10-dimethyl-7-aza-dispiro[3.0.4.1]decane-8-carboxylicacid[(1R,2S)-1-(pyrrolidine-1-sulfonylaminocarbonyl)-2-vinyl-cyclopropyl]-amide(0.040 g; 0.054 mmol) the reaction mixture was stirred overnight andpurified without workup by preparative HPLC (method L) to yield thetitle compound. HPLC (method A3) Rt=5.69 min; MS (method E): M/z=863[M+1]; 1H-NMR (500 MHz, DMSO-d6): 0.84 (s, 3H), 0.86 (s, 3H), 0.95 (s,9H), 0.96-1.23 (m, 7H), 1.23-1.27 (m, 2H), 1.35-1.50 (m, 2H), 1.55-2.00(m, 19H), 2.09-2.17 (m, 1H), 2.81-2.88 (m, 1H), 3.23-3.36 (m, 6H), 3.54(dd, 2H), 3.99 (dd, 1H), 4.13 (dd, 1 H), 4.41 (dd, 1H), 4.55 (d, 1H),5.10 (dd, 2H), 5.51 (ddd, 1H), 8.04 (d, 1H), 8.72 (d, 1H), 9.49 (bs,1H), 10.17 (bs, 1H).

Example 17 Compound 135

Step a[(S)—((S)-1-{(5R,8S)-10,10-Dimethyl-8-[(1R,2S)-1-(pyrrolidine-1-sulfonylaminocarbonyl)-2-vinyl-cyclopropylcarbamoyl]-7-aza-dispiro[3.0.4.1]decane-7-carbonyl}-2,2-dimethyl-propylcarbamoyl)-(1-methyl-cyclohexyl)-methyl]-carbamicacid tert-butyl ester

A solution of (S)-tert-Butoxycarbonylamino-(1-methyl-cyclohexyl)-aceticacid (0.217 g; 0.80 mmol) (prepared according to Tetrahedron Let. 2007,48, 6343-6347) and HATU (0.38 g; 1.00 mmol) in DCM (10 mL) was stirredfor 20 min at ambient temperature. After addition of DIPEA (0.698 mL;4.00 mmol) and(5R,8S)-7-((S)-2-Amino-3,3-dimethyl-butyryl)-10,10-dimethyl-7-aza-dispiro[3.0.4.1]decane-8-carboxylicacid[(1R,2S)-1-(pyrrolidine-1-sulfonylaminocarbonyl)-2-vinyl-cyclopropyl]-amide(0.400 g; 0.67 mmol) in DCM (10 mL) the reaction mixture was stirred for15 h, the solvent was removed in vacuo and the residue was purified bypreparative HPLC (method L) to yield the title compound. LC-MS (methodE): Rt=2.91 min; M/z=818 [M+H], HPLC (method A3) Rt=7.18 min

Step b(5R,8S)-7-{(S)-2-[(S)-2-Amino-2-(1-methyl-cyclohexyl)-acetylamino]-3,3-dimethyl-butyryl}-10,10-dimethyl-7-aza-dispiro[3.0.4.1]decane-8-carboxylicacid[(1R,2S)-1-(pyrrolidine-1-sulfonylaminocarbonyl)-2-vinyl-cyclopropyl]-amide

A mixture of[(S)—((S)-1-{(5R,8S)-10,10-Dimethyl-8-[(1R,2S)-1-(pyrrolidine-1-sulfonylaminocarbonyl)-2-vinyl-cyclopropylcarbamoyl]-7-aza-dispiro[3.0.4.1]decane-7-carbonyl}-2,2-dimethyl-propylcarbamoyl)-(1-methyl-cyclohexyl)-methyl]-carbamicacid tert-butyl ester (0.219 g; 0.27 mmol) and 2.0 mL HCl (4 M indioxane) in 2 mL dioxane was stirred at ambient temperature for 2 h. Themixture was concentrated under reduced pressure and co-evaporated 2times with DCM to yield the title compound which was used in the nextstep without further purification. LC-MS (method E): Rt=1.64 min;M/z=717 [M+]; HPLC (method A3): Rt=4.82 min

Step c

A solution of (S)-1-isopropyl-piperidine-2-carboxylic acid (0.014 g;0.080 mmol) and HATU (0.038 g; 0.100 mmol) in DMF (2 mL) was stirred for30 min at ambient temperature. After addition of DIPEA (0.070 mL; 0.398mmol) and((5R,8S)-7-{(S)-2-[(S)-2-Amino-2-(1-methyl-cyclohexyl)-acetylamino]-3,3-dimethyl-butyryl}-10,10-dimethyl-7-aza-dispiro[3.0.4.1]decane-8-carboxylicacid[(1R,2S)-1-(pyrrolidine-1-sulfonyl-aminocarbonyl)-2-vinyl-cyclopropyl]-amide(0.050 g; 0.066 mmol) the reaction mixture was stirred for 3 h andpurified without workup by preparative HPLC (method L) to yield thetitle compound. HPLC (method A3) Rt=5.40 min; MS (method E): M/z=870[M+]; 1H-NMR (500 MHz, DMSO-d6): 0.82 (s, 3H), 0.83 (s, 3H), 0.91 (s,3H), 0.94 (s, 9H), 1.15-1.35 (m, 11H), 1.39-1.55 (m, 6H), 1.65-1.85 (m,12H), 2.09-2.17 (m, 1H), 2.79-2.86 (m, 1H), 3.24-3.36 (m, 6H), 3.23-3.36(m, 6H), 3.40-3.51 (m, 3H), 3.53-3.55 (m, 2H), 4.52-4.58 (m, 2H), 5.15(dd, 2H), 5.50 (ddd, 1H), 8.00 (d, 1H), 8.62 (d, 1H), 9.50 (bs, 1H),10.19 (bs, 1H).

Example 18 Compound 147

Step a[(S)-2-{(5R,8S)-10,10-Dimethyl-8-[(1R,2S)-1-(pyrrolidine-1-sulfonylaminocarbonyl)-2-vinyl-cyclopropyl-carbamoyl]-7-aza-dispiro[3.0.4.1]dec-7-yl}-1-(4-methyl-tetrahydro-pyran-4-yl)-2-oxo-ethyl]-carbamicacid tert-butyl ester

A solution of(S)-tert-Butoxycarbonylamino-(4-methyl-tetrahydro-pyran-4-yl)-aceticacid (0.306 g; 1.12 mmol) (prepared according to Tetrahedron Let 2007,48, 6343-6347) and HATU (0.581 g; 1.53 mmol) in DCM (20 mL) was stirredfor 10 min at ambient temperature. DIPEA (1.05 mL; 6.11 mmol) and(5R,8S)-10,10-Dimethyl-7-aza-dispiro[3.0.4.1]decane-8-carboxylic acid[(1R,2S)-1-(pyrrolidine-1-sufonylaminocarbonyl)-2-vinyl-cyclopropyl]-amide(0.57 g; 1.02 mmol) were added, the reaction mixture was stirredovernight and purified without workup by preparative HPLC (method L) toyield the title compound. LC-MS (method E): Rt=2.55 min; M/z=706 [M+];HPLC (method A3): Rt=6.16 min

Step b(5R,8S)-7-[(S)-2-Amino-2-(4-methyl-tetrahydro-pyran-4-yl)-acetyl]-]-10,10-dimethyl-7-aza-dispiro-[3.0.4.1]decane-8-carboxylicacid[(1R,2S)-1-(pyrrolidine-1-sulfonylaminocarbonyl)-2-vinyl-cyclopropyl]-amide

A mixture of[(S)-2-{(5R,8S)-10,10-Dimethyl-8-[(1R,2S)-1-(pyrrolidine-1-sulfonylaminocarbonyl)-2-vinyl-cyclopropyl-carbamoyl]-7-aza-dispiro[3.0.4.1]dec-7-yl}-1-(4-methyl-tetrahydro-pyran-4-yl)-2-oxo-ethyl]-carbamicacid tert-butyl ester (0.415 g; 0.588 mmol) and 13.0 mL HCl (4 M indioxane) in 10 mL dioxane was stirred overnight at ambient temperature.The mixture was concentrated under reduced pressure to yield the titlecompound which was used in the next step without further purification.LC-MS (method E): Rt=1.45 min; M/z=606 [M+]; HPLC (method A3): Rt=4.01min

Step c[(S)-[(S)-2-{(5R,8S)-10,10-Dimethyl-8-[(1R,2S)-1-(pyrrolidine-1-sulfonylaminocarbonyl)-2-vinyl-cyclopropylcarbamoyl]-7-aza-dispiro[3.0.4.1]dec-7-yl}-2-oxo-1-(tetrahydro-pyran-4-yl)-ethylcarbamoyl]-(1-methyl-cyclohexyl)-methyl]-carbamicacid tert-butyl ester

A solution of (S)-tert-Butoxycarbonylamino-(1-methyl-cyclohexyl)-aceticacid (0.15 g; 0.55 mmol) (prepared according to Tetrahedron Let. 2007,48, 6343-6347) and HATU (0.31 g; 0.82 mmol) in DCM (15 mL) was stirredfor 30 min at ambient temperature. After addition of DIPEA (0.56 mL;3.27 mmol) and(5R,8S)-7-[(S)-2-Amino-2-(4-methyl-tetrahydro-pyran-4-yl)-acetyl]-10,10-dimethyl-7-aza-dispiro-[3.0.4.1]decane-8-carboxylicacid[(1R,2S)-1-(pyrrolidine-1-sulfonylaminocarbonyl)-2-vinyl-cyclopropyl]-amide(0.412 g; 0.55 mmol) in DCM (5 mL) the reaction mixture was stirred for3 h, the solvent was removed in vacuo and the residue was purified bypreparative HPLC (method L) to yield the title compound. LC-MS (methodE): Rt=2.78 min; M/z=859 [M+], HPLC (method A3) Rt=6.81 min

Step d(5R,8S)-7-[(S)-2-[(S)-2-Amino-2-(1-methyl-cyclohexyl)-acetylamino]-2-(4-methyl-tetrahydro-pyran-4-yl)-acetyl]-10,10-dimethyl-7-aza-dispiro[3.0.4.1]decane-8-carboxylicacid [(1R,2S)-1-(pyrrolidine-1-sulfonylamin

A mixture of[(S)-[(S)-2-{(5R,8S)-10,10-Dimethyl-8-[(1R,2S)-1-(pyrrolidine-1-sulfonylaminocarbonyl)-2-vinyl-cyclopropylcarbamoyl]-7-aza-dispiro[3.0.4.1]dec-7-yl}-2-oxo-1-(tetrahydro-pyran-4-yl)-ethylcarbamoyl]-(1-methyl-cyclohexyl)-methyl]-carbamicacid tert-butyl ester (0.227 g; 0.264 mmol) and 1.3 mL HCl (4 M indioxane) in 2 mL dioxane was stirred overnight at ambient temperature.The mixture was concentrated under reduced pressure to yield the titlecompound which was used in the next step without further purification.LC-MS (method E): Rt=1.59 min; M/z=759 [M+]; HPLC (method A3): Rt=4.58min

Step e

A solution of (S)-1-isopropyl-piperidine-2-carboxylic acid (0.011 g;0.053 mmol) and HATU (0.031 g; 0.080 mmol) in DMF (2 mL) was stirred for30 min at ambient temperature. DIPEA (0.055 mL; 0.32 mmol) and(5R,8S)-7-[(S)-2-[(S)-2-Amino-2-(1-methyl-cyclohexyl)-acetylamino]-2-(4-methyl-tetrahydro-pyran-4-yl)-acetyl]-10,10-dimethyl-7-aza-dispiro[3.0.4.1]decane-8-carboxylicacid[(1R,2S)-1-(pyrrolidine-1-sulfonylamino-carbonyl)-2-vinyl-cyclopropyl]-amide(0.050 g; 0.053 mmol) were added, the reaction mixture was stirredovernight and purified without workup by preparative HPLC (method L) toyield the title compound. LC-MS (method E): Rt=1.71 min; M/z=913 [M+H];HPLC (method A3): Rt=5.11 min

Example 19 Compound 149

Step a(5R,8S)-7-[(S)-2-(S)-2-Amino-2-cyclohexyl-acetylamino)-3,3-dimethyl-butyryl]-10,10-dimethyl-7-aza-dispiro[3.0.4.1]decane-8-carboxylicacid methyl ester

A mixture of(5R,8S)-7-[(S)-2-((S)-2-tert-Butoxycarbonylamino-2-cyclohexyl-acetylamino)-3,3-dimethyl-butyryl]-10,10-dimethyl-7-aza-dispiro[3.0.4.1]decane-8-carboxylicacid methyl ester (0.755 g; 1.31 mmol) and 4.9 mL HCl (4 M in dioxane)in 10 mL dioxane was stirred overnight at ambient temperature. Themixture was concentrated under reduced pressure to yield the titlecompound which was used in the next step without further purification.LC-MS (method E): Rt=1.47 min; M/z=476 [M+]; HPLC (method A3): Rt=4.27min

Step b(5R,8S)-7-((S)-2-{(S)-2-Cyclohexyl-2-[((S)-1-isopropyl-piperidine-2-carbonyl)-amino]-acetylamino}-3,3-dimethyl-butyryl)-10,10-dimethyl-7-aza-dispiro[3.0.4.1]decane-8-carboxylicacid methyl ester

A solution of (S)-1-isopropyl-piperidine-2-carboxylic acid (0.497 g;2.90 mmol) and HATU (1.65 g; 4.35 mmol) in DCM (100 mL) was cooled to 0°C. and(5R,8S)-7-[(S)-2-((S)-2-Amino-2-cyclohexyl-acetylamino)-3,3-dimethyl-butyryl]-10,10-dimethyl-7-aza-dispiro[3.0.4.1]decane-8-carboxylicacid methyl ester (1.65 g; 2.90 mmol) and DIPEA (2.98 mL; 17.4 mmol)were added. The reaction mixture was stirred for 3 h at room temperaturequenched with saturated aqueous bicarbonate. The aq. phase was extractedtwice with DCM, the combined organic phases dried with Na₂SO₄, filteredand the solvent was removed in vacuo. The product was purified bypreparative HPLC (method L) to yield the title compound. LC-MS (methodE): Rt=1.62 min; M/z=629 [M+]; HPLC (method A3): Rt=5.01 min

Step c(5R,8S)-7-((S)-2-{(S)-2-Cyclohexyl-2-[((S)-1-isopropyl-piperidine-2-carbonyl)-amino]-acetylamino}-3,3-dimethyl-butyryl)-10,10-dimethyl-7-aza-dispiro[3.0.4.1]decane-8-carboxylicacid

To a solution of(5R,8S)-7-((S)-2-{(S)-2-Cyclohexyl-2-[((S)-1-isopropyl-piperidine-2-carbonyl)-amino]-acetylamino}-3,3-dimethyl-butyryl)-10,10-dimethyl-7-aza-dispiro[3.0.4.1]decane-8-carboxylicacid methyl ester (0.69 g; 1.10 mmol) in THF/Methanol/water (2:1:1; 20mL) was added LiOH monohydrate (0.138 g; 3.3 mmol) and the reaction wasstirred overnight at room temperature. The solvent was removed in vacuo,water was added, the product was frozen in liquid nitrogen andlyophilized overnight to yield the title compound. LC-MS (method E):Rt=1.50 min; M/z=615 [M+]; HPLC (method A3): Rt=4.38 min

Step d

A solution of(5R,8S)-7-((S)-2-{(S)-2-Cyclohexyl-2-[((S)-1-isopropyl-piperidine-2-carbonyl)-amino]-acetylamino}-3,3-dimethyl-butyryl)-10,10-dimethyl-7-aza-dispiro[3.0.4.1]decane-8-carboxylicacid (0.040 g; 0.065 mmol) and HATU (0.050 g; 0.130 mmol) in DMF (2 mL)was stirred for 30 min at ambient temperature. After addition of DIPEA(0.057 mL; 0.325 mmol) and (D10)-Diethylamino-1-sulfonic acid((1R,2S)-1-amino-2-vinyl-cyclopropanecarbonyl)-amide (0.040 g; 0.130mmol) (prepared analogously as described for Intermediate III startingfrom commercially available deuterated d10-diethylamine) in DMF (2 mL)the reaction mixture was stirred overnight and purified without workupby preparative HPLC (method L) to yield the title compound. LC-MS(method E): Rt=1.76 min; M/z=869 [M+H], HPLC (method A3) Rt=5.78 min;1H-NMR (500 MHz, DMSO-d6): 1H-NMR (500 MHz, DMSO-d6): 0.79-0.87 (m, 9H),0.92-0.96 (m, 9H), 1.00-1.18 (m, 6H), 1.22-1.29 (m, 1H), 1.32-1.39 (m,1H), 1.43-1.51 (m, 2H), 1.53-1.73 (m, 11H), 1.74-1.93 (m, 8H), 2.05-2.14(m, 2H), 2.66-2.74 (m, 1H), 2.77 (dd, 1H), 2.66-1.74 (m, 1H), 2.89 (dd,1H), 3.53 (dd, 2H), 4.11 (dd, 1H), 4.36 (dd, 1H), 4.50 (d, 1H), 5.15(dd, 2H), 5.54 (ddd, 1H), 7.40 (d, 1H), 7.92 (d, 1H), 8.76 (s, 1H),10.15 (s, 1H).

Additional compounds of the invention are provided in Table A. Compounds1-203 have been prepared by methods of Examples 1 to 19 or by syntheticprocedures which are analogous to the procedures used in Examples 1 to19. Physical characterizing data and biological data for each compoundof Table A is provided in Table C.

TABLE A Cmpd. # Structure Name 1

tert-butyl [(1S)-1-{[(5R,8S)- 10,10-dimethyl-8-({(1R,2S)-1-[(pyrrolidin-1- ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}carbamoyl)-7-azadispiro[3.0.4.1]dec-7- yl]carbonyl}-2,2- dimethylpropyl]carbamate 2

tert-butyl [(1S)-1-{[(1S)-1- {[(5R,8S)-10,10-dimethyl-8-({(1R,2S)-1-[(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}carbamoyl)-7- azadispiro[3.0.4.1]dec-7-yl]carbonyl}-2,2- dimethylpropyl]carbamoyl}-2,2-dimethylpropyl]carbamate 3

(5R,8S)-7-[(2S)-2-{[(2S)-2- ({[(2S)-1-isopropylpiperidin-2-yl]carbonyl}amino)-3,3- dimethylbutanoyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 4

(5R,8S)-7-[(2S)-2-{[(2S)-1- ({[(3R)-1-ethylpiperidin-3-yl]carbonyl}amino)-3,3- dimethylbutanoyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 5

tert-butyl [(1S)-1-{[(1S)-1- {[(5R,8S)-10,10-dimethyl-8-({(1R,2S)-1-[(morpholin-4- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}carbamoyl)-7- azadispiro[3.0.4.1]dec-7-yl]carbonyl}-2,2- dimethylpropyl]carbamoyl}-2,2-dimethylpropyl]carbamate 6

(5R,8S)-7-[(2S)-2-{[(2S)-2- ({[(2S)-1-isopropylpiperidin-2-yl]carbonyl}amino)-3,3- dimethylbutanoyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(morpholin-4-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 7

(5R,8S)-7-[(2S)-2-{[(2S)-2- ({[(3R)-1-ethylpiperidin-3-yl]carbonyl}amino)-3,3- dimethylbutanoyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(morpholin-4-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 8

(5R,8S)-7-[(2S)-2-{[(2S)-2- ({[(2S)-1-(2- fluoroethyl)piperidin-2-yl]carbonyl}amino)-3,3- dimethylbutanoyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(morpholin-4-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 9

(5R,8S)-7-[(2S)-2-{[(2S)-3,3- dimethyl-2-(2-oxopyrrolidin-1-yl)butanoyl]amino}-3,3- dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1-[(pyrrolidin-1- ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 10

(5R,8S)-7-[(2S)-2-({(2S)-3,3- dimethyl-2-[(2-methyl-2- pyrrolidin-1-ylpropanoyl)amino]butanoyl}a mino)-3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 11

(5R,8S)-7-[(2S)-2-{[(2S)-2- ({[(2S)-1-isopropylpyrrolidin-2-yl]carbonyl}amino)-3,3- dimethylbutanoyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 12

(5R,8S)-7-[(2S)-2-{[(2S)-2- ({[(2S)-1-isopropylazetidin-2-yl]carbonyl}amino)-3,3- dimethylbutanoyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 13

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 14

(5R,8S)-7-[(2S)-2-({(2S)-2- cyclohexyl-2-[(2-methyl-2- pyrrolidin-1-ylpropanoyl)amino]acetyl}amino)- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 15

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpyrrolidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 16

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2R)-1-isopropylpyrrolidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 17

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1- isopropylazetidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 18

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2R)-1- isopropylazetidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 19

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-{[(1- isopropylazetidin-3-yl)carbonyl]amino}acetyl]amino}- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 20

(5R,8S)-7-[(2S)-2-{[(2S)-2- ({[(2S)-1-(2- fluoroethyl)piperidin-2-yl]carbonyl}amino)-3,3- dimethylbutanoyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 21

(5R,8S)-7-[(2S)-2-{[(2S)-2- ({[(2R)-1-isopropylpyrrolidin-2-yl]carbonyl}amino)-3,3- dimethylbutanoyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 22

(5R,8S)-7-[(2S)-2-{[(2S)-2- ({[(2R)-1-isopropylazetidin-2-yl]carbonyl}amino)-3,3- dimethylbutanoyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 23

(5R,8S)-7-[(2S)-2-{[(2S)-2-{[(1- isopropylazetidin-3-yl)carbonyl]amino}-3,3- dimethylbutanoyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 24

(5R,8S)-7-[(2S)-2-({(2S)-3,3- dimethyl-2-[(2-methyl-2- piperidin-1-ylpropanoyl)amino]butanoyl}a mino)-3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 25

(5R,8S)-7-[(2S)-2-({(2S)-2- cyclohexyl-2-[(2-methyl-2- piperidin-1-ylpropanoyl)amino]acetyl}amino)- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 26

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-(2-fluoroethyl)piperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 27

(5R,8S)-7-[(2S)-2-{[(2S)-2- ({[(2S)-1-cyclopentylpyrrolidin-2-yl]carbonyl}amino)-3,3- dimethylbutanoyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 28

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-cyclopentylpyrrolidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 29

(5R,8S)-7-[(2S)-2-{[(2S)-3,3- dimethyl-2-{[(6S)-4,5,6,7-tetrahydro-1H-imidazo[3,4- c]pyridin-6- ylcarbonyl]amino}butanoyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 30

(5R,8S)-N-{(1R,2R)-2-ethyl-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]cycloprop yl}-7-[(2S)-2-{[(2S)-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)-3,3-dimethylbutanoyl]amino}-3,3- dimethylbutanoyl]-10,10- dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 31

(5R,8S)-7-[(2S)-2-{[(2S)-2- ({[(2S)-1-cyclopentylpiperidin-2-yl]carbonyl}amino)-3,3- dimethylbutanoyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 32

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-cyclopentylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 33

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-(2-methoxyethyl)piperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 34

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- {(1R,2R)-2-ethyl-1-[(pyrrolidin- 1-ylsulfonyl)carbamoyl]cyclo- propyl}-10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 35

(5R,8S)-7-[(2S)-2-cyclohexyl- 2-{[(2S)-2-cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}acetyl]-10,10-dimethyl-N- {(1R,2S)-1-[(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 36

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2R)-1- ethylpiperidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 37

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1- ethylpiperidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 38

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2R)-1- ethylpyrrolidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 39

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1- ethylpyrrolidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 40

(5R,8S)-7-[(2S)-2-{[(2S)-2-{[(1- tert-butylazetidin-2-yl)carbonyl]amino}-2- cyclohexylacetyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 41

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-2-(tetrahydro-2H-pyran-4- yl)acetyl]-10,10-dimethyl-N-{(1R,2S)-1-[(pyrrolidin-1- ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 42

(5R,8S)-7-[(2S)-2-({(2S)-2- cyclohexyl-2-[(pyrazin-2-ylcarbonyl)amino]acetyl}amino)- 2-(tetrahydro-2H-pyran-4-yl)acetyl]-10,10-dimethyl-N- {(1R,2S)-1-[(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 43

(5R,8S)-7-[(2S)-3,3-dimethyl- 2-{[(2S)-2-[(pyrazin-2-ylcarbonyl)amino]-2- (tetrahydro-2H-pyran-4- yl)acetyl]amino}butanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 44

(5R,8S)-7-[(2S)-2-{[(2S)-2- ({[(2S)-1-isopropylpiperidin-2-yl]carbonyl}amino)-2- (tetrahydro-2H-pyran-4- yl)acetyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 45

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1-({[(3R)-3- fluoropyrrolidin-1-yl]sulfonyl}carbamoyl)-2- vinylcyclopropyl]-10,10- dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 46

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1-({[(3S)-3- fluoropyrrolidin-1-yl]sulfonyl}carbamoyl)-2- vinylcyclopropyl]-10,10- dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 47

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2R)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 48

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2R)-1- methylpiperidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 49

(5R,8S)-N-[(1R,2S)-1- ({[cyclobutyl(methyl)amino]sulfo-nyl}carbamoyl)-2- vinylcyclopropyl]-7-[(2S)-2-{[(2S)-2-cyclohexyl-2-({[(2S)-1- isopropylpiperidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 50

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1- ({[(cyclopropylmethyl)(methyl)amino]sulfonyl}carbamoyl)-2- vinylcyclopropyl]-10,10- dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 51

(5R,8S)-7-[(2S)-2-{[3,3- dimethyl-2-(pyridin-3-ylamino)butanoyl]amino}-3,3- dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 52

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-[(1R,2S)-1-({[methyl(phenyl)amino]sulfonyl} carbamoyl)-2- vinylcyclopropyl]-7-azadispiro[3.0.4.1]decane-8- carboxamide 53

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1- ({[cyclopropyl(methyl)amino]sul-fonyl}carbamoyl)-2- vinylcyclopropyl]-10,10- dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 54

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1-({[cyclopropyl(2-methoxyethyl)amino]sulfonyl}car- bamoyl)-2-vinylcyclopropyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 55

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1- ({[methoxy(methyl)amino)sulfonyl}carbamoyl)-2- vinylcyclopropyl]-10,10- dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 56

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1-({[(2-methoxyethyl)(methyl)amino]sul- fonyl}carbamoyl)-2-vinylcyclopropyl]-10,10- dimethyl-7- azadispiro[3.0.4.1]decane-8-carboxamide 57

(5R,8S)-N-[(1R,2S)-1- {[(cyclobutylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]-7- [(2S)-2-{[(2S)-2-cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8-carboxamide 58

(5R,8S)-7-[(2S)-2-{[(2S)-2- cylcopentyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsuflonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 59

(5R,8S)-7-[(2S)-2-{[(2S)-2- cylcopentyl-2-({[(2S)-1-isopropylpyrrolidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 60

(5R,8S)-7-[(2S)-2-({[1-(2- amino-2- oxoethyl)cyclohexyl]acetyl}amino)-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 61

(5R,8S)-7-[(2S)-2-({[1- (cyanomethyl)cyclohexyl]acetyl} amino)-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 62

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[2S)-1-isopropylpyrrolidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1- {[(diethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]- 10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 63

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1- ethylpyrrolidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-N- [(1R,2S)-1-{[(diethylamino)sulfonyl]carba moyl}-2-vinylcyclopropyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 64

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-cyclopentylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1- {[(diethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]- 10,10-dimethyl-7-azaidspiro[3.0.4.1]decane-8- carboxamide 65

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2R)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1- {[(diethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]- 10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 66

(5R,8S)-7-[(2S)-2-{[(2S)-2- cylcohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-2-cyclopentylacetyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 67

(5R)-7-[(2S)-2-[(N-{[(2S)-1- isopropylpiperidin-2-yl]carbonyl}-3-methyl-L- valyl)amino]-2-(tetrahydro-2H-pyrazn-4-yl)acetyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 68

N-[(1S)-1-{[(5R)-10,10- dimethyl-8-({(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}carbamoyl)-7-azadispiro[3.0.4.1]dec-7- yl]carbonyl}-2,2- dimethylpropyl]-N′-propylisophthalamide 69

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[6- (dimethylamino)pyridin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 70

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[2- (dimethylamino)pyridin-3-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 71

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-(2,2,2-trifluoroethyl)pyrrolidin-2- yl]carbonyl}-amino)acetyl]amino}-2-(tetrahydro-2H-pyran-4- yl)acetyl]-10,10-dimethyl-N-{(1R,2S)-1-[(pyrrolidin-1- ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 72

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-(2,2-difluoroethyl)pyrrolidin-2- yl]carbonyl}amino)acetyl]amino}-2-(tetrahydro-2H-pyran-4- yl)acetyl]-10,10-dimethyl-N-{(1R,2S)-1-[(pyrrolidin-1- ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 73

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-(2-fluoroethyl)pyrrolidin-2- yl]carbonyl}amino)acetyl]amino}-2-(tetrahydro-2H-pyran-4- yl)acetyl]-10,10-dimethyl-N-{(1R,2S)-1-[(pyrrolidin-1- ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 74

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-(2,2-difluoroethyl)piperidin-2- yl]carbonyl}amino)acetyl]amino}-2-(tetrahydro-2H-pyran-4- yl)acetyl]-10,10-dimethyl-N-{(1R,2S)-1-[(pyrrolidin-1- ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 75

(5R,8S)-7-[(2S)-2-{[(2S)-2- cylcohexyl-2-({[(2S)-1-(2-fluoroethyl)piperidin-2- yl]carbonyl}amino)acetyl]amino}-2-(tetrahydro-2H-pyran-4- yl)acetyl]-10,10-dimethyl-N-{(1R,2S)-1-[(pyrrolidin-1- ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 76

2-fluoroethyl (2S)-2-{[(1S)-1- cyclohexyl-2-{[(1S)-2-[(5R,8S)-10,10-dimethyl-8-({(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}carbamoyl)-7- azadispiro[3.0.4.1]dec-7-yl]-2-oxo-1-(tetrahydro-2H-pyran-4- yl)ethyl]amino}-2-oxoethyl]carbamoyl}pyrrolidine- 1-carboxylate 77

(5R,8S)-7-[(2S)-2-{[(2S)-2- cylcohexyl-2-({[(2S)-1- ethylpiperidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-N- [(1R,2S)-1-{[(diethylamino)sulfonyl]carba moyl}-2-vinylcyclopropyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 78

(5R)-7-[(2S)-3,3-dimethyl-2- {[(2-oxopiperidin-3-yl)carbonyl]amino}butanoyl]- 10,10-dimethyl-N-{(1R,2S)-1-[(pyrrolidin-1- ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 79

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclopentyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1- {[(diethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]- 10,10-dimethyl-7-azadiaspiro[3.0.4.1]decane-8- carboxamide 80

(5R,8S)-7-[(2S)-2-{[(2S)-2- cylcohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-2-cyclopentylacetyl]-N- [(1R,2S)-1- {[(diethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]- 10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 81

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclopentyl-2-({[(2S)-1- ethylpiperidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-N- [(1R,2S)-1-{[(diethylamino)sulfonyl]carba moyl}-2-vinylcyclopropyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 82

(5R,8S)-7-[(2S)-2-{[(2S)-2- cylcohexyl-2-({[(2S)-1- methylpiperidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-2- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 83

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethybutanoyl]-N- [(1R,2S)-1-({[(2,2-difluoroethyl)(methyl)amino]sul fonyl}carbamoyl)-2-vinylcyclopropyl]-10,10- dimethyl-7- azadispiro[3.0.4.1]decane-8-carboxamide 84

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-2-(tetrahydro-2H-pyran-4- yl)acetyl]-N-[(1R,2S)-1-{[(diethylamino)sulfonyl]carba moyl}-2-vinylcyclopropyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 85

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1- ethylpiperidin-2-yl]carbonyl}amino)acetyl]amino}- 2-(tetrahydro-2H-pyran-4-yl)acetyl]-N-[(1R,2S)-1- {[(diethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]- 10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 86

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1- ethylpiperidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-N- [(1R,2R)-1-{[(diethylamino)sulfonyl]carba moyl}-2-ethylcyclopropyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 87

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1- ethylpiperidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-N-{(1R,2R)-2-ethyl-1-[(pyrrolidin- 1- ylsulfonyl)carbamoyl]cyclo-propyl}-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 88

N-[(1S)-1-{[(5R)-10,10- dimethyl-8-({(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}carbamoyl)-7-azadispiro[3.0.4.1]dec-7- yl]carbonyl}-2,2- dimethylpropyl]-N′-methylisophthalamide 89

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-4,4-difluoro-1-isopropylpyrrolidin- 2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 90

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2R)-1- ({[cyclopropyl(methyl)amino]sul-fonyl}carbamoyl)-2- ethylcyclopropyl]-10,10- dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 91

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpyrrolidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1- ({[ethyl(methyl)amino]sulfonyl}carbamoyl)-2- vinylcyclopropyl]-10,10- dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 92

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2R)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1- ({[ethyl(methyl)amino]sulfonyl}carbamoyl)-2- vinylcyclopropyl]-10,10- dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 93

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1- methylpiperidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-N- [(1R,2S)-1-({[ethyl(methyl)amino]sulfonyl} carbamoyl)-2- vinylcyclopropyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 94

(5R,8S)-7-[(2S)-2-{[(2S)-2- cylcohexyl-2-({[(2S)-1- ethylpiperidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-N- [(1R,2S)-1-({[ethyl(methyl)amino]sulfonyl} carbamoyl)-2- vinylcyclopropyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 95

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1- ethylpyrrolidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(piperidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 96

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1- ethylpyrrolidin-2-yl]carbonyl}amino)acetyl]amino}- 2-(tetrahydro-2H-pyran-4-yl)acetyl]-N-[(1R,2S)-1- {[(diethylamino)sulfonyl)carbamoyl}-2-vinylcyclopropyl]- 10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 97

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclopentyl-2-({[(2S)-1- ethylpyrrolidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-N- [(1R,2S)-1-{[(diethylamino)sulfonyl]carba moyl}-2-vinylcyclopropyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 98

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1- ethylpyrrolidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-[(1R,2S)-1- ({[methyl(propyl)amino]sulfonyl}carbamoyl)-2- vinylcyclopropyl]-7- azadispiro[3.0.4.1]decane-8-carboxamide 99

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1- ethylpyrrolidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-N-{(1R,2R)-2-ethyl-1-[(pyrrolidin- 1- ylsulfonyl)carbamoyl]cyclo-propyl}-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 100

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1- ethylpyrrolidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-N- [(1R,2R)-1-{[(diethylamino)sulfonyl]carba moyl}-2-ethylcyclopropyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 101

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1- ethylpyrrolidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-N- [(1R,2S)-1-({[ethyl(methyl)amino]sulfonyl} carbamoyl)-2- vinylcyclopropyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 102

(5R,8S)-7-[(2S)-2-{[(2S)-2- ({[(2S)-1-ethylpyrrolidin-2-yl]carbonyl}amino)-2- phenylacetyl]amino}-3,3- dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 103

(5R,8S)-7-[(2S)-2-{[(2S)-2- ({[(2S)-1-ethylpiperidin-2-yl]carbonyl}amino)-2- phenylacetyl]amino}-3,3- dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 104

(5R,8S)-7-[(2S)-2-{[(2S)-2- ({[(2S)-1-isopropylpiperidin-2-yl]carbonyl}amino)-2- phenylacetyl]amino}-3,3- dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 105

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-5,5-difluoro-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 106

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1- ({[ethyl(propyl)amino]sulfonyl}carbamoyl)-2-vinylcyclopropyl]- 10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 107

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1- ethylpyrrolidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-N- [(1R,2S)-1-({[ethyl(propyl)amino]sulfonyl} carbamoyl)-2-vinylcyclopropyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 108

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1- ({[isopropyl(methyl)amino]sulfonyl}carbamoyl)-2- vinylcyclopropyl]-10,10- dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 109

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1- ethylpyrrolidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-N- [(1R,2S)-1-({[isopropyl(methyl)amino]sulfo nyl}carbamoyl)-2-vinylcyclopropyl]-10,10- dimethyl-7- azadispiro[3.0.4.1]decane-8-carboxamide 110

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1- ({[ethyl(isopropyl)amino]sulfonyl}carbamoyl)-2- vinylcyclopropyl]-10,10- dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 111

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1- ethylpyrrolidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-N- [(1R,2S)-1-({[ethyl(isopropyl)amino]sulfo- nyl}carbamoyl)-2-vinylcyclopropyl]-10,10- dimethyl-7- azadispiro[3.0.4.1]decane-8-carboxamide 112

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-[(1R,2S)-1-({[methyl(propyl)amino]sulfonyl} carbamoyl)-2- vinylcyclopropyl]-7-azadispiro[3.0.4.1]decane-8- carboxamide 113

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-{(1R,2S)-1- [(piperidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 114

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2R)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-[(1R,2S)-1-({[methyl(propyl)amino]sulfonyl} carbamoyl)-2- vinylcyclopropyl]-7-azadispiro[3,0.4.1]decane-8- carboxamide 115

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2R)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-{(1R,2S)-1- [(piperidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 116

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpyrrolidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- {(1R,2R)-2-ethyl-1-[(pyrrolidin- 1-ylsulfonyl)carbamoyl]cyclo- propyl}-10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 117

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpyrrolidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2R)-1- {[(diethylamino)sulfonyl]carbamoyl}-2-ethylcyclopropyl]- 10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 118

(5R,8S)-7-[(2S)-2-{[(2S)-2- cylcohexyl-2-({[(2S)-1- methylpiperidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-N- [(1R,2S)-1-{[(diethylamino)sulfonyl]carba moyl}-2-vinylcyclopropyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 119

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2R)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1- ({[isopropyl(methyl)amino]sulfonyl}carbamoyl)-2- vinylcyclopropyl]-10,10- dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 120

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2R)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1- ({[ethyl(isopropyl)amino]sulfo-nyl}carbamoyl)-2- vinylcyclopropyl]-10,10- dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 121

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2R)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2R)-1- {[(diethylamino)sulfonyl]carbamoyl}-2-ethylcyclopropyl]- 10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 122

(5R,8S)-N-[(1R,2S)-1- {[(diethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]-7- [(2S)-2-{[(2S)-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)-3- methylbutanoyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-7- azadispiro[3.0.4.1]decane-8-carboxamide 123

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2R)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- {(1R,2R)-2-ethyl-1-[(pyrrolidin- 1-ylsulfonyl)carbamoyl]cyclo- propyl}-10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 124

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-2-(4-methyltetrahydro-2H- pyran-4-yl)acetyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 125

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1- ethylpyrrolidin-2-yl]carbonyl}amino)acetyl]amino}- 2-(4-methyltetrahydro-2H-pyrazn-4-yl)acetyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 126

1-ethyl-L-prolyl-N-[(1S)-2- [(5R,8S)-10,10-dimethyl-8-({(1R,2S)-1-[(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}carbamoyl)-7- azadispiro[3.0.4.1]dec-7-yl]-1-(4-methyltetrahydro-2H-pyran- 4-yl)-2-oxoethyl]-3-methyl-L- valinamide127

(5R,8S)-7-[(2S)-2-{[(2S)-2- ({[(2S)-1-isopropylpiperidin-2-yl]carbonyl}amino)-2- (tetrahydro-2H-pyran-4- yl)acetyl]amino}-2-(4-methyltetrahydro-2H-pyran-4- yl)acetyl]-10,10-dimethyl-N-{(1R,2S)-1-[(pyrrolidin-1- ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 128

(5R,8S)-7-[(2S)-2-[(N-{[(2S)-1- isopropylpiperidin-2-yl]carbonyl}-3-methyl-L- valyl)amino]-2-(4- methyltetrahydro-2H-pyran-4-yl)acetyl]-10,10-dimethyl-N- {(1R,2S)-1-[(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 129

(5R,8S)-7-[(2S)-2-{[(2S)-2- ({[(2S)-1-ethylpyrrolidin-2-yl]carbonyl}amino)-2- (tetrahydro-2H-pyran-4- yl)acetyl]amino}-2-(4-methyltetrahydro-2H-pyran-4- yl)acetyl]-10,10-dimethyl-N-{(1R,2S)-1-[(pyrrolidin-1- ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 130

(5R,8S)-N-[(1R,2S)-1- {[(diethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]-7- [(2S)-2-{[(2S)-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)-3- methylbutanoyl]amino}-3-methylbutanoyl]-10,10- dimethyl-7- azadispiro[3.0.4.1]decane-8-carboxamide 131

(5R,8S)-N-[(1R,2S)-1- {[(diethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]-7- [(2S)-2-{[(2S)-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)-3,3- dimethylbutanoyl]amino}-3-methylbutanoyl]-10,10- dimethyl-7- azadispiro[3.0.4.1]decane-8-carboxamide 132

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3-methylbutanoyl]-N- [(1R,2S)-1- {[(diethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]- 10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 133

(5R,8S)-N-[(1R,2S)-1- {[(diethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]-7- [(2S)-2-{[(2S)-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)-2-(1-methylcyclohexyl)acetyl]amino}- 3,3-dimethylbutanol]-10,10- dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 134

(5R,8S)-N-[(1R,2S)-1- {[(diethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]-7- [(2S)-2-{[(2S)-2-({[(2S)-1-ethylpyrrolidin-2- yl]carbonyl}amino)-2-(1-methylcyclohexyl)acetyl]amino}- 3,3-dimethylbutanoyl]-10,10- dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 135

(5R,8S)-7-[(2S)-2-{[(2S)-2- ({[(2S)-1-isopropylpiperidin-2-yl]carbonyl}amino)-2-(1- methylcyclohexyl)acetyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 136

(5R,8S)-7-[(2S)-2-{[(2S)-2- ({[(2S)-1-ethylpyrrolidin-2-yl]carbonyl}amino)-2-(1- methylcyclohexyl)acetyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 137

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2R)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1- ({[ethyl(propyl)amino]sulfonyl}car-bamoyl)-2-vinylcyclopropyl]- 10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 138

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-d5-ethylpyrrolidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide-d5 139

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-d5- ethylpiperidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide-d5 140

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-d7-isopropylpyrrolidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide-d7 141

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2R)-2-ethyl-1-({[isopropyl(methyl)amino]sulfo nyl}carbamoyl)cyclopropyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 142

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2R)-2-ethyl-1-({[methyl(propyl)amino]sulfonyl} carbamoyl)cyclopropyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 143

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1-{[(3,3- difluoropyrrolidin-1-yl)sulfonyl]carbamoyl}-2- vinylcyclopropyl]-10,10- dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 144

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-3-ethyl-1,3-thiazolidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 145

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide-d7 146

(5R,8S)-7-[(2S)-2-{[(2S)-2- ({[(2S)-1-ethylpyrrolidin-2-yl]carbonyl}amino)-2-(1- methylcyclohexyl)acetyl]amino}-2-(4-methyltetrahydro-2H- pyran-4-yl)acetyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 147

(5R,8S)-7-[(2S)-2-{[(2S)-2- ({[(2S)-1-isopropylpiperidin-2-yl]carbonyl}amino)-2-(1- methylcyclohexyl)acetyl]amino}-2-(4-methyltetrahydro-2H- pyran-4-yl)acetyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 148

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1-{[(d6- dimethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]- 10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide-d6 149

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1-{[(d10-diethylamino)sulfonyl]carbamoyl}- 2-vinylcyclopropyl]-10,10- dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide-d10 150

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-2-(4-methyltetrahydro-2H- pyran-4-yl)acetyl]-N-[(1R,2S)- 1-{[(diethylamino)sulfonyl)carba moyl}-2-vinylcyclopropyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 151

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1- ethylpiperidin-2-yl]carbonyl}amino)acetyl]amino}- 2-(4-methyltetrahydro-2H-pyran-4-yl)acetyl]-N-[(1R,2S)- 1- {[(diethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]- 10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 152

(5R,8S)-N-[(1R,2S)-1- {[(diethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]-7- [(2S)-2-{[(2S)-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)-2-(1-methylcyclohexyl)acetyl]amino}- 2-(4-methyltetrahydro-2H-pyrazn-4-yl)acetyl]-10,10- dimethyl-7- azadispiro[3.0.4.1]decane-8-carboxamide 153

(5R,8S)-N-[(1R,2S)-1- {[(diethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]-7- [(2S)-2-{[(2S)-2-({[(2S)-1-ethylpyrrolidin-2- yl]carbonyl}amino)-2-(1-methylcyclohexyl)acetyl]amino}- 2-(4-methyltetrahydro-2H-pyrazn-4-yl)acetyl]-10,10- dimethyl-7- azadispiro[3.0.4.1]decane-8-carboxamide 154

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1- ethylpyrrolidin-2-yl]carbonyl}amino)acetyl]amino}- 2-(4-methyltetrahydro-2H-pyran-4-yl)acetyl]-N-[(1R,2S)- 1- {[(diethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]- 10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 155

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1-({[(2,2-difluoroethyl)(ethyl)amino]sulfo nyl}carbamoyl)-2-vinylcyclopropyl]-10,10- dimethyl-7- azadispiro[3.0.4.1]decane-8-carboxamide 156

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanol]-N- [(1R,2S)-1-({[ethyl(2-fluoroethyl)amino]sulfonyl}carba- moyl)-2-vinylcyclopropyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 157

(5R,8S)-N-[(1R,2S)-1- {[(diethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]-7- [(2S)-2-{[(2S)-2-({[(2S)-1-ethylpyrrolidin-2- yl]carbonyl}amino)-2-(4- methyltetrahydro-2H-pyran-4-yl)acetyl]amino}-2-(1- methylcyclohexyl)acetyl]- 10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 158

(5R,8S)-N-[(1R,2S)-1- {[(diethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]-7- [(2S)-2-{[(2S)-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)-2-(4-methyltetrahydro-2H-pyran-4- yl)acetyl]amino}-2-(1-methylcyclohexyl)acetyl]- 10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8-carboxamide 159

(5R,8S)-N-[(1R,2S)-1- {[(diethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]-7- [(2S)-2-{[(2S)-2-({[(2S)-1-ethylpyrrolidin-2- yl]carbonyl}amino)-2-(1-methylcyclohexyl)acetyl]amino}- 2-(1- methylcyclohexyl)acetyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 160

(5R,8S)-N-[(1R,2S)-1- {[(diethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]-7- [(2S)-2-{[(2S)-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)-2-(1-methylcyclohexyl)acetyl]amino}- 2-(1- methylcyclohexyl)acetyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 161

(5R,8S)-7-[(2S)-2-{[(2S)-2-{[3- acetyl-4,5-dimethyl-1H-pyrrol-2-yl)carbonyl]amino}-3,3- dimethylbutanoyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 162

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-{[(1- isopropylpiperidin-2-yl)carbonyl]amino}acetyl]amino}- 3,3-dimethylbutanoyl]-N- [(1R,2S)-1-{[(dimethylsmino)sulfonyl]carba- moyl}-2-vinylcyclopropyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 163

(5R,8S)-N-[1-({[(2S)-2- (hydroxymethyl)pyrrolidin-1-yl]sulfonyl}carbamoyl)-2- vinylcyclopropyl]-7-[(2S)-2-{[(2S)-2-{[(1-isopropylpiperidin- 2-yl)carbonyl]amino}-3,3-dimethylbutanoyl]amino}-3,3- dimethylbutanoyl]-10,10- dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 164

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-{[(1- isopropylpiperidin-2-yl)carbonyl]amino}acetyl]amino}- 3,3-dimethylbutanoyl]-N-(1-{[(3,3-difluoroazetidin-1- yl)sulfonyl]carbamoyl}-2-vinylcyclopropyl)-10,10- dimethyl-7- azadispiro[3.0.4.1]decane-8-carboxamide 165

(5R,8S)-7-[(2S)-2-({(2S)-2- cyclohexyl-2-[(pyrazin-2-ylcarbonyl)amino]acetyl}amino)- 3,3-dimethylbutanoyl]-N- [(1R,2S)-1-{[(cyclopropylamino)sulfonyl]car- bamoyl}-2-vinylcyclopropyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 166

(5R,8S)-N-[(1R,2S)-1-{[(tert- butylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]-7-[(2S)-2- ({(2S)-2-cyclohexyl-2- [(pyrazin-2-ylcarbonyl)amino]acetyl}amino)- 3,3-dimethylbutanoyl]-10,10- dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 167

(5R,8S)-7-[(2S)-2-({(2S)-2- cyclohexyl-2-[(pyrazin-2-ylcarbonyl)amino]acetyl}amino)- 3,3-dimethylbutanoyl]-N- [(1R,2S)-1-({[ethyl(methyl)amino]sulfonyl} carbamoyl)-2- vinylcyclopropyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 168

(5R,8S)-N-[(1R,2S)-1-({[(2- chloroethyl)(methyl)amino]sulfo-nyl}carbamoyl)-2- vinylcyclopropyl]-7-[(2S)-2- ({(2S)-2-cyclohexyl-2-[(pyrazin-2- ylcarbonyl)amino]acetyl}amino)-3,3-dimethylbutanoyl]-10,10- dimethyl-7- azadispiro[3.0.4.1]decane-8-carboxamide 169

(5R,8S)-N-[(1R,2S)-1-{[(tert- butylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]-7-[(2S)-2- {[(2S)-2-cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]- 10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8-carboxamide 170

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1- ({[ethyl(methyl)amino]sulfonyl}carbamoyl)-2- vinylcyclopropyl]-10,10- dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 171

(5R,8S)-N-[(1R,2S)-1-({[(2- chloroethyl)(methyl)amino]sulfo-nyl}carbamoyl)-2- vinylcyclopropyl]-7-[(2S)-2-{[(2S)-2-cyclohexyl-2-({[(2S)-1- isopropylpiperidin-2-yl]carbonyl}amino)acetyl]amino}- 3,3-dimethylbutanoyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 172

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1- {[(cyclopropylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]- 10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 173

(5R,8S)-7-[(2S)-2-({(2S)-2- cyclohexyl-2-[(pyrazin-2-ylcarbonyl)amino]acetyl}amino)- 3,3-dimethylbutanoyl]-N- [(1R,2S)-2-{[(diethylamino)sulfonyl]carba moyl}-2-vinylcyclopropyl]-10,10-dimethyl-7- azadispiro[3.0.4.1]decane-8- carboxamide 174

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N- [(1R,2S)-1- {[(diethylamino)sulfonyl]carbamoyl}-2-vinylcyclopropyl]- 10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide 175

(5R,8S)-7-[(2S)-2- ({cyclohexyl[(pyridin-4-ylacetyl)amino]acetyl}amino)- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 176

(5R,8S)-7-{(2S)-2- [(cyclohexyl{[(5-methoxy-1H- indol-2-yl)carbonyl]amino}acetyl)amino]- 3,3-dimethylbutanoyl}-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 177

(5R,8S)-7-[(2S)-2- ({cyclohexyl[(3,4- dihydroisoquinolin-2(1H)-ylacetyl)amino]acetyl}amino)- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 178

(5R,8S)-7-{(2S)-2- [(cyclohexyl{[(1-methyl-1H- indol-2-yl)carbonyl]amino}acetyl)amino]- 3,3-dimethylbutanoyl}-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 179

(5R,8S)-7-[(2S)-2- ({cyclohexyl[(tetrahydro-2H- pyran-2-ylacetyl)amino]acetyl}amino)- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 180

(5R,8S)-7-{(2S)-2- [(cyclohexyl{[(1-ethyl-3-methyl- 1H-pyrazol-5-yl)carbonyl]amino}acetyl)amino]- 3,3-dimethylbutanoyl}-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 181

(5R,8S)-7-[(2S)-2-{[{[(3-tert- butyl-1-methyl-1H-pyrazol-5-yl)carbonyl]amino}(cyclohexyl) acetyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 182

(5R,8S)-7-{(2)-2- [(cyclohexyl{[2- (methylamino)benzoyl]amino}acetyl)amino]-3,3- dimethylbutanoyl}-10,10- dimethyl-N-{(1R,2S)-1-[(pyrrolidin-1- ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 183

(5R,8S)-7-[(2S)-2-{[{[(1-tert- butyl-3-methyl-1H-pyrazol-5-yl)carbonyl]amino}(cyclohexyl) acetyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 184

(5R,8S)-7-{(2S)-2- [(cyclohexyl{[(1-phenyl-1H- pyrazol-4-yl)carbonyl]amino}acetyl)amino]- 3,3-dimethylbutanoyl}-10,10-dimethyl-N-[(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 185

(5R,8S)-7-{(2S)-2- [(cyclohexyl{[(3-ethyl-1-methyl- 1H-pyrazol-5-yl)carbonyl]amino}acetyl)amino]- 3,3-dimethylbutanoyl}-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 186

(5R,8S)-7-{(2S)-2- [(cyclohexyl{[(3,5-dimethyl-1H- pyrazol-1-yl)acetyl]amino}acetyl)amino]- 3,3-dimethylbutanoyl}-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 187

(5R,8S)-7-[(2S)-2-{[({[(2S)-1- acetylpyrrolidin-2-yl]carbonyl}amino)(cyclohexyl) acetyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 188

(5R,8S)-7-[(2S)-2- ({cyclohexyl[(1H-indol-2-ylcarbonyl)amino]acetyl}amino)- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 189

(5R,8S)-7-[(2S)-2- ({cyclohexyl[(1H-indol-3-ylcarbonyl)amino]acetyl}amino)- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 190

(5R,8S)-7-[(2S)-2- ({cyclohexyl[(1H-indol-5-ylcarbonyl)amino]acetyl}amino)- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 191

(5R,8S)-7-[(2S)-2-({[(1- benzofuran-2- ylcarbonyl)amino](cyclohexyl)acetyl}amino)-3,3- dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1-[(pyrrolidin-1- ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 192

(5R,8S)-7-[(2S)-2-({[(1- benzofuran-5- ylcarbonyl)amino](cyclohexyl)acetyl}amino)-3,3- dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1-[(pyrrolidin-1- ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 193

(5R,8S)-7-{(2S)-2- [(cyclohexyl{[(2S)-2-methoxy- 2-phenylacetyl]amino}acetyl)ami no]-3,3-dimethylbutanoyl}-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 194

(5R,8S)-7-[(2S)-2-{[{[(1- acetylpiperidin-4-yl)carbonyl]amino}(cyclohexyl) acetyl]amino}-3,3-dimethylbutanoyl]-10,10- dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1-ylsulfonyl)carbamoyl]-2- vinylcyclopropyl}-7-azadispiro[3.0.4.1]decane-8- carboxamide 195

(5R,8S)-7-[(2S)-2- ({cyclohexyl[(isoquinolin-1-ylcarbonyl)amino]acetyl}amino)- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 196

(5R,8S)-7-[(2S)-2- ({cyclohexyl[(quinolin-3-ylcarbonyl)amino]acetyl}amino)- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 197

(5R,8S)-7-[(2S)-2- ({cyclohexyl[(quinolin-4-ylcarbonyl)amino]acetyl}amino)- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 198

(5R,8S)-7-{(2S)-2- [(cyclohexyl{[(1-methyl-1H- indol-5-yl)carbonyl]amino}acetyl)amino]- 3,3-dimethylbutanoyl}-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 199

(5R,8S)-7-{(2S)-2- [(cyclohexyl{[(5-methylpyrazin- 2-yl)carbonyl]amino}acetyl)amino]- 3,3-dimethylbutanoyl}-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 200

(5R,8S)-7-{(2S)-2- [(cyclohexyl{[(dimethylamino)acetyl]amino}acetyl)amino]-3,3- dimethylbutanoyl}-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 201

(5R,8S)-7-[(2S)-2- ({cyclohexyl[(1,2,5-oxadiazol- 3-ylcarbonyl)amino]acetyl}amino)- 3,3-dimethylbutanoyl]-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 202

(5R,8S)-7-{(2S)-2- [(cyclohexyl{[(4- methylpiperazin-1-yl)acetyl]amino}acetyl)amino]- 3,3-dimethylbutanoyl}-10,10-dimethyl-N-{(1R,2S)-1- [(pyrrolidin-1- ylsulfonyl)carbamoyl]-2-vinylcyclopropyl}-7- azadispiro[3.0.4.1]decane-8- carboxamide 203

(5R,8S)-7-[(2S)-2-{[(2S)-2- cyclohexyl-2-({[(2S)-1-isopropylpiperidin-2- yl]carbonyl}amino)acetyl]amino}-3,3-dimethylbutanoyl]-N-(1- {[(diethylamino)sulfonyl]carbamoyl}-2-ethylcyclopropyl)- 10,10-dimethyl-7-azadispiro[3.0.4.1]decane-8- carboxamide

The compounds listed in Table B are also embodiments of the invention.

TABLE B Compound Structure No.

204

205

206

207

208

209

210

211

212

213

214

215

Biological Activity Example 20 HCV NS3-4A Protease Assay

The inhibitory activity of certain compounds of Table A against HCVNS3-4A serine protease is determined in a homogenous assay using thefull-length NS3-4A protein (genotype 1a, strain HCV-1) and acommercially available internally-quenched fluorogenic peptide substrateas described by Taliani, M., et al. 1996 Anal. Biochem. 240:60-67, whichis incorporated by reference in its entirety.

Example 21 Luciferase-Based HCV Replicon Assay

The antiviral activity and cytotoxicity of certain compounds of Table Ais determined using a subgenomic genotype 1b HCV replicon cell line(Huh-Luc/neo-ET) containing a luciferase reporter gene, the expressionof which is under the control of HCV RNA replication and translation.Briefly, 5,000 replicon cells are seeded in each well of 96-well tissueculture plates and are allowed to attach in complete culture mediawithout G418 overnight. On the next day, the culture media are replacedwith media containing a serially diluted compound of Table A in thepresence of 10% FBS and 0.5% DMSO. After a 48-h treatment with thecompound of Table A, the remaining luciferase activities in the cellsare determined using BriteLite reagent (Perkin Elmer, Wellesley, Mass.)with a LMaxII plate reader (Molecular Probe, Invitrogen). Each datapoint represents the average of four replicates in cell culture. IC₅₀ isthe concentration of the at which the luciferase activity in thereplicon cells is reduced by 50%. The cytotoxicity of the compound ofTable A is evaluated using an MTS-based cell viability assay.

Compounds in Table A supra have been tested in the protease assay ofExample 20. The IC₅₀ values for each compound are provided in Table C.Compounds of Table A supra may have also been tested in the repliconassay of Example 21 and exhibit an IC₅₀ of less than about 100 nM orless.

TABLE C Protease Com- assay pound Ex. 12 LC- Retention MS- Mass NumberIC50 (μM) Method time method observed Ion 1 0.4 I3 3.73 I3 664.3 M + H 20.75 I3 3.75 I3 777.4 M + H 3 0.006 B 3.57 J 830.5 M + H 4 0.035 I3 2.92I3 816.5 M + H 5 6.65 I3 3.65 I3 791.3 M − H 6 0.045 I 2.86 I 846.4 M +H 7 0.45 I 2.76 I 832.5 M + H 8 0.3 I 2.84 I 850.5 M + H 9 0.1 I 3.61 I745.5 M + H 10 0.065 B 3.59 J 816.4 M + H 11 0.02 B 3.59 J 817.5 M + H12 0.04 B 3.54 J 802.5 M + H 13 0.003 D 2.13 E 856.5 M + H 14 0.003 B3.65 J 842.5 M + H 15 0.002 B 3.65 J 842.5 M + H 16 0.0023 B 3.62 J842.5 M + H 17 0.0025 B 3.63 J 828.4 M + H 18 0.01 B 3.63 J 828.4 M + H19 0.055 B 3.6 J 828.5 M + H 20 0.07 B 3.52 J 834.5 M + H 21 0.035 B3.52 J 816.4 M + H 22 0.095 B 3.46 J 802.4 M + H 23 0.4 B 3.49 J 802.4M + H 24 0.065 B 3.56 J 830.5 M + H 25 0.008 B 3.64 J 856.5 M + H 260.015 B 3.62 J 860.5 M + H 27 0.01 B 3.62 J 842.3 M + H 28 0.002 B 3.7 J868.5 M + H 29 0.04 B 3.11 J 826.3 M + H 30 0.062 B 3.61 J 832.5 M + H31 0.008 B 3.65 J 856.6 M + H 32 0.001 B 3.74 J 880.5 M + H 33 0.0035 B3.65 J 872.5 M + H 34 0.0045 B 3.7 J 858.5 M + H 35 0.003 B 3.83 G 882.4M + H 36 0.0035 A3 5.11 E 842.3 M + H 37 0.0033 A3 5.15 E 842.3 M + H 380.0035 A3 5.07 E 828.3 M + H 39 0.0025 A3 5.07 E 828.3 M + H 40 0.006 A35.16 E 842.3 M + H 41 0.0009 A3 4.82 E 884.18 M+ 42 0.04 A3 5.854 E837.04 M+ 43 0.06 A3 5.549 E 811 M+ 44 0.015 A3 4.6 E 858.14 M− 45 0.001A3 5.113 J 874.16 M + H 46 0.002 A3 5.086 J 874.16 M + H 47 0.0048 B3.65 J 856.5 M + H 48 0.0009 B 3.54 J 828.5 M + H 49 0.0033 A3 5.536 E870.2 M+ 50 0.0038 A3 5.402 E 870.2 M+ 51 1.15 B 3.61; 3.67 J 754.5 M +H 52 0.0025 A3 5.501 E 892.2 M+ 53 0.0017 A3 5.257 E 856.17 M+ 54 0.0025A3 5.258 E 900.22 M+ 55 0.0014 B 3.61 E 846.4 M + H 56 0.008 A3 5.078 E874.18 M+ 57 0.0065 A3 5.247 E 856.17 M+ 58 0.0035 D 2.104 E 842.5 M + H59 0.0035 D 2.088 E 828.4 M + H 60 1.25 D 2.535 E 756.5 M + H 61 0.75 D2.734 E 727.5 M + H 62 0.001 B 3.7 E 844.5 M + H 63 0.0012 B 3.66 E830.5 M + H 64 0.002 B 3.83 E 884.5 M + H 65 0.0045 B 3.7 E 858.5 M + H66 0.0055 B 3.8 E 868.3 M + H 67 0.02 A3 4.817 E 858.14 M+ 68 0.95 A35.987 E 752.96 M+ 69 0.05 B 4.73 J 851.5 M + H 70 0.035 B 3.56 J 851.5M + H 71 0.04 A3 6.279 M 910.1 M + H 72 0.07 A3 4.937 M 892.11 M + H 730.015 A3 4.692 M 874.12 M + H 74 0.065 A3 4.84 E 906.13 M + H 75 0.03 A34.731 E 888.14 M + H 76 0.08 A3 5.972 E 918.13 M + H 77 0.0009 B 3.72 E844.3 M + H 78 0.65 A3 5.11/5.26 E 688.88 M+ 79 0.0025 B 4.422 H 842.5 M− H 80 0.002 B 4.503 H 868.5 M − H 81 0.004 B 4.378 H 828.4 M − H 820.0025 B 3.91 J 828.5 M + H 83 0.002 A3 5.25 E 880.14 M + H 84 0.006 B4.017 H 884.5 M − H 85 0.0045 B 4.013 H 870.4 M − H 86 0.0045 B 4.252 H844.5 M − H 87 0.007 D 2.267 E 844.5 M + H 88 0.5 A3 5.545 E 724.91 M+89 0.03 A3 5.747 E 878.12 M+ 90 0.0065 A3 5.319 E 858.18 M+ 91 0.005 B3.61 J 830.5 M + H 92 0.003 B 3.61 J 844.5 M + H 93 0.002 B 3.57 J 816.4M + H 94 0.0015 B 3.61 J 830.5 M + H 95 0.005 D 2.41 E 842.5 M + H 960.007 B 3.664 H 856.5 M − H 97 0.01 B 3.484 H 814.3 M − H 98 0.007 D2.26 E 830.5 M + H 99 0.02 D 2.093 E 830.5 M + H 100 0.01 B 3.813 H830.5 M − H 101 0.0025 B 3.72 J 816.4 M + H 102 0.008 B 3.651 H 820.3 M− H 103 0.02 B 3.81 H 834.4 M − H 104 0.015 B 3.738 H 848.3 M − H 1050.045 A3 5.385 E 892.15 M+ 106 0.01 B 3.84 B 872.5 M + H 107 0.009 B3.76 E 844.5 M + H 108 0.006 B 3.69 E 858.4 M + H 109 0.0025 B 3.66 E830.3 M + H 110 0.008 B 3.8 E 872.5 M + H 111 0.008 B 3.74 E 844.5 M + H112 0.0014 B 3.72 J 858.5 M + H 113 0.0035 B 3.77 J 870.5 M + H 1140.0045 B 3.7 J 858.5 M + H 115 0.0045 B 3.7 J 870.5 M + H 116 0.0045 B3.67 J 844.5 M + H 117 0.0055 B 3.76 J 846.5 M + H 118 0.0045 B 3.66 J830.5 M + H 119 0.0065 B 3.68 E 858.5 M + H 120 0.01 B 3.75 E 872.5 M +H 121 0.007 B 3.72 J 860.5 M + H 122 0.0014 D 2.07 E 818.5 M + H 1230.008 B 3.69 E 858.5 M + H 124 0.0015 A3 4.892 E 898.21 M − H 125<0.0003 A3 4.761 E 870.15 M+ 126 0.006 A3 4.58 E 844.12 M − H 127 0.004A3 4.327 E 900.18 M − H 128 0.0014 A3 4.742 E 872.17 M − H 129 0.006 A34.161 E 872.13 M − H 130 0.008 D 2.002 E 804.4 M + H 131 0.0055 D 2.053E 818.5 M + H 132 0.0028 E 844.5 M + H 133 0.003 A3 5.574 E 872.21 M+134 0.005 A3 5.427 E 844.16 M+ 135 0.0045 A3 5.401 E 870.2 M+ 136 0.007A3 5.27 E 842.14 M+ 137 0.0035 B 3.83 E 872.5 M + H 138 0.003 A3 5.552 E833.15 M+ 139 0.0035 A3 5.589 E 847.17 M + H 140 0.0025 A3 5.592 E849.19 M + H 141 0.008 B 3.62 E 860.7 M + H 142 0.01 B 3.64 E 860.7 M +H 143 0.003 A3 5.33 E 892.15 M+ 144 0.009 A3 5.24/5.33 E 846.15 M+ 1450.0059 A3 5.688 E 863.21 M + H 146 0.003 A3 4.944 E 884.18 M+ 147 0.0015A3 5.115 E 912.23 M+ 148 0.0008 A3 5.447 E 836.17 M + H 149 0.0015 A35.783 E 868.25 M + H 150 0.0024 A3 5.541 E 900.22 M + H 151 0.002 A35.446 E 886.19 M + H 152 0.0011 A3 5.624 E 914.25 M + H 153 0.0018 A35.496 E 886.19 M + H 154 0.0028 A3 5.365 E 872.17 M + H 155 0.0044 A35.394 E 894.17 M − H 156 0.0013 A3 5.246 E 876.18 M − H 157 0.001 A35.217 E 886.19 M − H 158 0.022 A3 5.331 E 914.25 M+ 159 0.011 A3 5.839 E884.22 M − H 160 0.003 A3 5.923 E 912.28 M − H 161 0.065 A5 1.63 A5840.5 M + H 162 0.0009 A4 1.48 A4 830.8 M + H 163 1.5 A4 1.27 A4 861.6M + H 164 0.008 A6 14.96 A6 879.6 M + H 165 0.0062 A5 1.49 A5 795.4 M +H 166 0.01 A5 1.55 A5 812.8 M + H 167 0.0006 A5 1.51 A5 798.7 M + H 1680.03 A5 1.51 A5 832.8 M + H 169 0.0015 A5 1.67 A5 860 M + H 170 0.0005A5 1.66 A5 845 M + H 171 0.001 A5 1.48 A5 879 M + H 172 0.0025 A5 1.42A5 842.9 M + H 173 0.003 A5 1.55 A5 812.7 M + H 174 0.0006 A4 1.61 A4858.6 M + H 175 0.01 A6 6.76 A6 822.46 M + H 176 0.025 A6 7.68 A6 876.47M + H 177 0.025 A6 8.22 A6 876.5 M + H 178 0.08 A6 8.14 A6 860.48 M + H179 0.025 A6 7.62 A6 829.49 M + H 180 0.03 A6 7.56 A6 839.48 M + H 1810.09 A6 8.13 A6 867.52 M + H 182 0.07 A6 8.09 A6 836.47 M + H 183 0.095A6 7.93 A6 867.52 M + H 184 0.035 A6 7.68 A6 873.47 M + H 185 0.04 A67.63 A6 839.49 M + H 186 0.065 A6 7.36 A6 839.49 M + H 187 0.025 A6 6.68A6 842.48 M + H 188 0.02 A6 7.79 A6 846.46 M + H 189 0.025 A6 7.35 A6846.46 M + H 190 0.02 A6 7.31 A6 846.46 M + H 191 0.055 A6 8.08 A6847.44 M + H 192 0.025 A6 7.75 A6 847.44 M + H 193 0.025 A6 7.91 A6851.47 M + H 194 0.01 A6 6.66 A6 856.5 M + H 195 0.075 A6 8.29 A6 858.46M + H 196 0.02 A6 7.51 A6 858.46 M + H 197 0.04 A6 7.35 A6 858.46 M + H198 0.04 A6 7.65 A6 860.47 M + H 199 0.014 A6 7.62 A6 823.45 M + H 2000.008 A6 7.02 A6 788.48 M + H 201 0.035 A6 6.78 A6 799.42 M + H 202 0.02A6 5.89 A6 843.52 M + H 203 0.008 A6 13.62 A6 860.2 M + H

Those skilled in the art will recognize, or be able to ascertain usingno more than routine experimentation, many equivalents to the specificembodiments and methods described herein. Such equivalents are intendedto be encompassed by the scope of the following claims.

1. A compound according to the Formula (I)

and pharmaceutically acceptable salts and stereoisomers thereof; whereinR is C₁-C₆alkyl, C₂-C₆alkenyl or C₃-C₇cycloalkylC₀-C₄alkyl; R′ ishydrogen or C₁-C₆alkyl; or R and R′, together with the carbon atom towhich they are attached, form a three to seven member carbocycle whichis saturated or partially unsaturated, which carbocycle is substitutedwith 0, 1, 2, or 3 residues independently selected from the groupconsisting of C₁-C₆alkyl, C₂-C₆alkenyl, C₁-C₄alkylidenyl, andC₃-C₇cycloalkylC₀-C₄alkyl; R₁ and R₂ are independently hydrogen or areindependently selected from the group consisting of C₁-C₆alkyl,C₁-C₆alkoxy and C₃-C₇cycloalkylC₀-C₂alkyl, each of which is substitutedwith 0, 1, or 2 residues selected from halogen and C₁-C₄alkyl; or R₁ andR₂, taken in combination with the N to which they are attached, form asaturated, unsaturated or aromatic heterocyclic ring having 0, 1, or 2additional ring heteroatoms independently selected from N, O, or S andwhich heterocyclic ring has from 4 to 7 total ring atoms, saidheterocycle having 0, 1, 2, or 3 substituents which are independentlyselected from C₁-C₄alkyl, halo C₁-C₄alkyl, C₂-C₄alkenyl, C₂-C₄alkynyl,hydroxyl, C₁-C₄alkoxy, haloC₁-C₄alkoxy, amino, mono- anddi-C₁₋₄alkylamino, aminoC₁-C₄alkyl, C₁-C₄alkanoylaminoC₁-C₄alkyl; R₄ isC₁-C₈alkyl, C₃-C₈cycloalkyl, or saturated 5 or 6 membered heterocyclicring having 1 or 2 ring heteroatoms independently selected from N, O orS, each of which is substituted with 0-2 C₁-C₄alkyl groups; J is a bondor a divalent residue of the formula:

R₅ is C₁-C₈alkyl, C₃-C₈cycloalkyl, or saturated 5 or 6 memberedheterocyclic ring having 1 or 2 ring heteroatoms independently selectedfrom N, O or S, each of which is substituted with 0-2 C₁-C₄alkyl groups;R₆ is hydrogen or C₁-C₄alkyl; G is a group of the formula -E-R₇; E is abond, CH₂, C(O), S(O)₂, C(R₉)₂C(O), or C(O)C(R₉)₂, R₇ is selected fromthe group consisting of C₁-C₆alkyl, haloC₁-C₆alkyl,C₃-C₇cycloalkylC₀-C₂alkyl, C₁-C₆alkoxy, haloC₁-C₆alkoxy,C₃-C₇cycloalkylC₀-C₂alkoxy, mono- and di-C₁-C₆alkylamino, —S(O)₂R₁₀,—N(R₉)S(O)₂R₁₀, monocyclic or bicyclic heterocycle, and monocyclic orbicyclic aryl, wherein each residue is unsubstituted or substituted with1, 2, or 3 R₈ groups each of which R₈ residues is independently selectedfrom the group consisting of C₁-C₆alkyl, and C₁-C₆alkanoyl; or R₆ andR₇, taken in combination with the N atom to which they are attached,forms a 4 to 7 membered heterocyclic ring having 0, 1, or 2 additionalring heteroatoms selected from N, O or S and which ring is substitutedby 0, 1, 2 or 3 substituents which are independently selected from thegroup consisting of oxo, C₁-C₄alkyl, halo C₁-C₄alkyl, C₂-C₄alkenyl,C₂-C₄alkynyl, hydroxyl, C₁-C₄alkoxy, haloC₁-C₄alkoxy, amino, mono- anddi-C₁₋₄alkylamino, aminoC₁-C₄alkyl, C₁-C₄alkanoylaminoC₁-C₄alkyl; R₉ isindependently selected at each occurrence from hydrogen and C₁-C₄alkyl;R₁₀ is C₁-C₆alkyl, amino or mono- and di-C₁-C₆alkylamino; andpharmaceutically acceptable salts, hydrates, and solvates thereof. 2.The compound of claim 1 of Formula (II):

wherein R₃ is C₁-C₆alkyl or C₂-C₆alkenyl.
 3. The compound of claim 1 ofFormula (III):

and pharmaceutically acceptable salts and stereoisomers thereof; whereinX is absent or selected from NR^(11a) or oxygen; i and k areindependently selected integers selected from the group consisting of 0,1, 2, 3 and 4; j is an integer selected from the group consisting of 1,2, 3 and 4, wherein the sum of i+j+k is less than or equal to 5 andgreater than or equal to 2 when X is absent and the sum of i+j+k is lessthan or equal to 4 and greater than or equal to 1 when X is oxygen; R¹¹represents zero to three residues each independently selected at eachoccurrence from the group consisting of halogen, hydroxy, amino,C₁₋₄alkyl, C₃₋₆cycloalkyl, C₁₋₄alkoxy, mono- and di-C₁₋₄alkylamino,hydroxyC₁₋₄alkyl, and C₁₋₄alkoxyC₁₋₄alkyl; and R^(11a) is independentlyselected at each occurrence from the group consisting of hydrogen,C₁₋₄alkyl, haloC₁₋₄alkyl, C₃₋₆cycloalkyl, hydroxyC₁₋₄alkyl, andC₁₋₄alkoxyC₁₋₄alkyl.
 4. The compound of claim 1 of Formula (IV):

and pharmaceutically acceptable salts and stereoisomers thereof; whereini is an integer selected from the group consisting of 0, 1, 2, 3 and 4;j is an integer selected from the group consisting of 1, 2, 3 and 4,wherein the sum of i+j is less than or equal to 5 and greater than orequal to 2; R¹¹ represents zero to three residues each independentlyselected at each occurrence from the group consisting of halogen,hydroxy, amino, C₁₋₄alkyl, C₃₋₆cycloalkyl, C₁₋₄alkoxy, mono- anddi-C₁₋₄alkylamino, hydroxyC₁₋₄alkyl, and C₁₋₄alkoxyC₁₋₄alkyl; andR^(11a) is independently selected at each occurrence from the groupconsisting of hydrogen, C₁₋₄alkyl, haloC₁₋₄alkyl, C₃₋₆cycloalkyl,hydroxyC₁₋₄alkyl, and C₁₋₄alkoxyC₁₋₄alkyl.
 5. The compound of claim 1 ofthe Formula (V):

and pharmaceutically acceptable salts and stereoisomers thereof; whereini is 0 or 1; and R^(11a) is hydrogen or C₁₋₄alkyl.
 6. The compound ofclaim 1, wherein J is a divalent residue of the formula:

wherein R₅ is C₁-C₆alkyl, C₄-C₇cycloalkyl, or saturated 5 or 6 memberedheterocyclic ring having 1 or 2 ring heteroatoms independently selectedfrom N, O or S, each of which is substituted with 0-2 C₁-C₄ alkylgroups.
 7. The compound of claim 1, wherein R₄ and R₅ are independentlyselected from the group consisting of tert-butyl, cyclohexyl,1-methyl-cyclohexyl, tetrahydropyran-4-yl and1-methyl-tetrahydropyran-4-yl.
 8. The compound of claim 1, wherein R₁and R₂ are independently selected from the group consisting of hydrogen,C₁-C₆alkyl, and C₃-C₇cycloalkylC₀-C₂alkyl, or R₁ and R₂ taken incombination with the N to which they are attached, form a saturated,unsaturated or aromatic heterocyclic ring having 0, 1, or 2 additionalring heteroatoms independently selected from N, O, or S and whichheterocyclic ring has from 4 to 7 total ring atoms, said heterocyclehaving 0, 1, 2, or 3 substituents which are independently selected fromC₁-C₄alkyl, halo C₁-C₄alkyl, C₂-C₄alkenyl, C₂-C₄alkynyl, hydroxyl,C₁-C₄alkoxy, haloC₁-C₄alkoxy, amino, mono- and di-C₁₋₄alkylamino,aminoC₁-C₄alkyl, C₁-C₄alkanoylaminoC₁-C₄alkyl.
 9. The compound of claim1, wherein R₁ and R₂ are independently selected from the groupconsisting of C₁-C₄alkyl, C₁-C₃alkyl substituted with one or morefluorine atoms, C₃-C₆cycloalkyl and cyclopropylmethyl; or R₁, R₂ and thenitrogen atom to which they are attached form a pyrrolidinyl ring, apiperidinyl ring or a morpholinyl ring.
 10. The compound of claim 1,wherein R is C₁-C₆alkyl, C₂-C₄alkenyl or C₃-C₆cycloalkylC₀-C₂alkyl; R′is hydrogen or C₁-C₄alkyl; or R and R′, together with the carbon atom towhich they are attached, form a cyclopropyl ring, which is substitutedwith 0 or 1 residues selected from the group consisting of C₁-C₄alkyl,C₂-C₄alkenyl, methylidene, and C₃-C₆cycloalkylC₀-C₂alkyl.
 11. Thecompound of claim 3, in which R_(11a) is selected from the groupconsisting of C₁-C₄alkyl and perdeuteroC₁-C₄alkyl.
 12. The compound ofclaim 3, in which R_(11a) is selected from the group consisting ofethyl, ethyl-d₅, isopropyl and isopropyl-d₇.
 13. A method of treating anHCV-associated disorder, comprising: administering to a subject in needthereof a pharmaceutically acceptable amount of the compound accordingto claim 1, such that the HCV-associated disorder is treated.
 14. Themethod of claim 13, wherein the HCV-associated disorder is selected fromthe group consisting of HCV infection, liver cirrhosis, chronic liverdisease, hepatocellular carcinoma, cryoglobulinaemia, non-Hodgkin'slymphoma, liver fibrosis and a suppressed innate intracellular immuneresponse.
 15. A method of treating, inhibiting or preventing theactivity of HCV or HIV in a subject in need thereof, comprising:administering to the subject a pharmaceutically acceptable amount of thecompound according to claim
 1. 16. A method of treating anHCV-associated disorder, comprising: administering to a subject in needthereof a pharmaceutically effective amount of a compound according toclaim 1, and a pharmaceutically effective amount of an additionalHCV-modulating compound, such that the HCV-associated disorder istreated.
 17. The method of claim 16, wherein the additionalHCV-modulating compound is selected from the group consisting of NIM811,ITMN191, MK-7009, TMC 435350, Sch 503034 and VX-950.
 18. The method ofclaim 16, wherein the additional HCV-modulating compound is interferonor derivatized interferon selected from the group consisting ofinterferon alpha 2B, pegylated interferon alpha, consensus interferon,interferon alpha 2A, lymphoblastoid interferon, and interferon tau; andsaid compound having anti-hepatitis C virus activity is selected fromthe group consisting of interleukin 2, interleukin 6, interleukin 12, acompound that enhances the development of a type 1 helper T cellresponse, double stranded RNA, double stranded RNA complexed withtobramycin, Imiquimod, ribavirin, an inosine 5′-monophosphatedehydrogenase inhibitor, amantadine, and rimantadine.
 19. The method ofclaim 16, wherein the additional HCV-modulating compound is a cytochromeP450 monooxygenase inhibitor selected from the group consisting ofritonavir, ketoconazole, troleandomycin, 4-methylpyrazole, cyclosporin,and clomethiazole.
 20. A pharmaceutically acceptable formulation for thetreatment of an HCV-associated disorder, on comprising: the compoundaccording to claim 1, and a pharmaceutically acceptable excipient.